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Lemon Bottle

A Korean 'fat-dissolving' solution injected in beauty clinics; the FDA calls it an unapproved drug, and it has no clinical trials.

A South Korean solution marketed for 'fat dissolving' and injected in aesthetic settings; its distributor calls it a cosmetic, Swissmedic classes the injected product as an unauthorised medicine, the FDA has called it an unapproved new drug, and no clinical trial has been registered.

Data refreshed 2026-09-23 · Based on 8 published references

At a glance

FDA approved
No.
Potential results
  • No study has tested this mix
  • Lecithin-based shots: thinner belly fat (small study, untreated side for comparison)
  • Lecithin-based shots: less chin fat (trial vs placebo)
  • Bromelain by mouth: less weight gain in mice (animal study only)

Unverified, online reports only: reducing fat on the double chin, jowls, lower cheeks, jaw, upper arms and abdomen.

Dose
Study doses: see the Scientific view
Converter: mg, mL and syringe units
Side effects and warnings
  • No side-effect data for Lemon Bottle have been published in medical journals. No trial has collected any.
  • The FDA warns about unapproved fat-dissolving shots in general (Lemon Bottle not named). It cites lasting scars, serious infections, skin damage, cysts and deep, painful lumps.
  • In April 2025, the UK pharmacy regulator said products like this may have caused serious harm.

A summary of the sources on this page, not medical advice.

Names

Also called: LemonBottle, LemonBottle Ampoule Solution, Lemon Bottle lipolysis solution

Regulatory (US)

FDA approval: none

503A compounding: unknown
Not on any FDA compounding list; see Regulatory picture.

Molecule

Origin

Developer: SID Medicos, Seoul, South Korea

What is inside

Lemon Bottle is a brand of liquid made by SID Medicos. The company is in Seoul, South Korea. It is sold online and on social media as a “fat dissolving” liquid. Sellers also call it a “lipolysis” (fat breakdown) solution. Regulators in Switzerland, the United States and the UK all say it is being injected. But the company that sells it told regulators it is a cosmetic, meant only for use on the skin.

The maker lists three main ingredients:

  • riboflavin (vitamin B2)
  • bromelain (enzymes from pineapple)
  • lecithin (a fatty substance from soybeans or egg yolk)

It also lists unnamed “natural ingredients”. The full recipe and the amounts are not published.

Nobody can be sure what is in a given pack. In 2024, the Swiss regulator tested samples from different sellers. It could not find the listed ingredients. One sample held only caffeine.

Declared composition, from packaging and marketing as summarised by Swissmedic: mainly bromelain, lecithin and riboflavin, plus several unspecified natural ingredients. No quantitative formula has been published, and the product has no PubChem, CAS or pharmacopoeial identity. Marketing quoted in FDA’s 2025 warning letters attributes the effect to lecithin breaking down fat-cell membranes and to riboflavin helping the body discharge dissolved fat faster than normal metabolism; those are the seller’s claims, not findings.

Analytical data: the official Swissmedic laboratory analysed samples of “Lemon Bottle” lipolysis solution obtained from various sources and reported in March 2024 that the ingredients did not match the declaration and varied greatly from pack to pack. In one sample the only substance found was caffeine; in another none of the listed ingredients could be detected. Swissmedic described these samples as falsifications. No independent peer-reviewed analysis, sterility or endotoxin testing, or stability data for authentic product were found, and nothing is known about the pharmacokinetics of any component after subcutaneous injection of this product.

Ingredient: Riboflavin

Riboflavin is vitamin B2. We get it from milk, eggs, meat and cereals with added vitamins. The body turns it into two helper molecules. Many enzymes need these helpers to get energy from food. This includes the enzymes that burn fat for fuel inside cells. Riboflavin is bright yellow, and light breaks it down.

The marketing claims lean on this normal role in the body. But that does not mean injecting it into a patch of fat breaks the fat down. It also does not mean the fat clears faster. No study was found that shows either effect. The FDA has approved riboflavin (in a form called riboflavin phosphate) in some products. These are multivitamins given into a vein, and eye drops used in an eye procedure. Neither one has anything to do with losing fat.

Riboflavin (7,8-dimethyl-10-D-ribityl-isoalloxazine, C17H20N4O6, 376.4 g/mol, PubChem CID 493570) is converted by riboflavin kinase and FAD synthetase to flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD). These are prosthetic groups of flavoproteins including respiratory-chain complexes I and II and the acyl-CoA dehydrogenases that catalyse the first step of mitochondrial fatty-acid β-oxidation. That is the intracellular oxidation of fatty acids already released from triglyceride; riboflavin is not a lipase, a detergent or an adipocytolytic agent. No evidence was found that extra riboflavin in a person who is not deficient increases fat oxidation, and PubMed contains no study of locally injected riboflavin reducing subcutaneous fat.

Riboflavin is water-soluble and photolabile. Its 5’-phosphate ester is the photosensitiser in Photrexa and Photrexa Viscous, FDA-approved in 2016 for corneal collagen cross-linking with ultraviolet light in progressive keratoconus, and is the riboflavin source in intravenous multivitamin products such as Infuvite Adult.

Ingredient: Bromelain

Bromelain is a mix of enzymes from the pineapple plant. These enzymes break down protein. It comes from the stem and the fruit. It is sold as a supplement. It is also used to make meat more tender. The FDA has approved one medicine made from pineapple-stem enzymes. It is called NexoBrid. It is a gel spread on bad burns for a few hours. It breaks down dead, burned tissue. It is not injected.

A 2012 lab study used mouse fat cells in dishes. Bromelain stopped young fat cells from growing up. It also made grown fat cells die and release their fat. This was only in lab dishes. No study was found that shows injecting bromelain into human fat reduces it. Nobody has studied what happens when this kind of enzyme is injected under human skin.

Bromelain is a crude extract of Ananas comosus containing several cysteine proteases, principally stem bromelain (EC 3.4.22.32) and fruit bromelain (EC 3.4.22.33), with smaller amounts of ananain and comosain; it is a protein mixture, not a single molecule. The enzymatic debriding agent anacaulase-bcdb (NexoBrid), a mixture of pineapple-stem enzymes, was approved by the FDA on 2022-12-28 as a topical gel applied for four hours to remove eschar in adults with deep partial-thickness or full-thickness thermal burns, based on two trials in 357 patients.

Adipocyte data: Dave et al. (PLoS One 2012) reported that stem bromelain irreversibly inhibited differentiation of 3T3-L1 preadipocytes by down-regulating C/EBPα and PPARγ, and in mature 3T3-L1 adipocytes induced apoptosis and lipolysis through Akt inhibition and augmented TNF-α signalling, with reduced perilipin and PDE3B expression. These are in-vitro findings in a mouse cell line at culture concentrations. No animal or human study of injected bromelain for localised fat reduction was found.

Ingredient: Lecithin

Lecithin is a name for a group of fatty substances. They are the main building blocks of the outer layer of cells. Most lecithin comes from soybeans, sunflower seeds and egg yolk. It is often added to food to keep oil and water mixed. Its main part is called phosphatidylcholine.

Phosphatidylcholine has long been used in “fat dissolving” shots. It is usually mixed with a bile salt called deoxycholate. The FDA says both are common in fat-dissolving shots that it has not approved. A 2004 lab study looked at these mixes. It found the fat-killing effect came mainly from the deoxycholate, not the phosphatidylcholine. Deoxycholate works a bit like soap. No study was found that shows lecithin shrinks fat when injected without a soap-like substance.

Lecithin is a mixture of glycerophospholipids, chiefly phosphatidylcholine (PC) with phosphatidylethanolamine, phosphatidylinositol and phosphatidic acid, whose proportions depend on source and fractionation; it has no single formula. PC is amphiphilic and does not dissolve in water as single molecules, so aqueous injectables require a solubiliser or form liposomes.

Rotunda et al. (Dermatol Surg 2004) compared a clinical PC injection, isolated sodium deoxycholate and the laboratory detergents Triton X-100 and Empigen BB in cell culture and porcine tissue. The PC formula and deoxycholate alone produced comparable loss of cell viability, membrane lysis and disruption of fat and muscle architecture, similar to the laboratory detergents. The authors concluded that the formula works primarily as a detergent causing nonspecific cell lysis and that deoxycholate is the major active component. Deoxycholic acid was later approved on its own as Kybella. The three declared main ingredients of Lemon Bottle do not include deoxycholate or another recognised detergent, so the mechanism established for PC–deoxycholate products does not carry over; the lecithin content and how it is solubilised are unpublished.

Why researchers might study these together

The maker explains the product as a chain of steps. Its ads, quoted in FDA warning letters, make two claims. They say lecithin breaks open fat cells. They say riboflavin helps the body get rid of the melted fat faster than normal. Bromelain, an enzyme that breaks down protein, is the third ingredient. Each step borrows a real fact about an ingredient. But nobody has tested whether these facts add up to melting fat under the skin.

No trial of Lemon Bottle is listed on ClinicalTrials.gov. No published study of the product was found in PubMed. The lab evidence on its ingredients comes down to two things. There is one study of bromelain in lab dishes. There is older work on phosphatidylcholine mixes. In that work, the fat-killing effect came from a soap-like salt that Lemon Bottle does not list. The mix of ingredients has never been tested in animals or people.

Framed as a hypothesis, the proposed mechanism has three parts: disruption of adipocyte membranes by phospholipid (lecithin), pro-apoptotic and lipolytic effects on adipocytes (bromelain, by analogy with the 3T3-L1 data of Dave et al., 2012), and faster oxidation of released fatty acids (riboflavin, by analogy with FAD’s role as cofactor of the acyl-CoA dehydrogenases). None of the three analogies has been tested in vivo for this purpose, and there is no published rationale for their combination or proportions.

The membrane-disruption step is the weakest link: in the PC–deoxycholate literature, cytolytic activity was attributed to the detergent rather than to PC (Rotunda et al., 2004), and no detergent is declared. The riboflavin step assumes that cofactor supply limits fat oxidation, for which no evidence in non-deficient tissue was found. The bromelain step extrapolates from a mouse cell line to human subcutaneous tissue. Finally, Swissmedic’s laboratory findings mean that even a well-designed study would first need to establish what the product actually contains. No trial is registered and no animal study of the product was found.

Regulatory picture

Approval: no medicine regulator has approved Lemon Bottle. In 2024, the company that sells it told the Swiss regulator the real product is a cosmetic. It said it is only for use on the skin. No approval in South Korea as a drug or medical device was found. No statement about it from South Korea’s drug safety agency was found either.

Regulators that have acted:

  • Switzerland (2024) said the injected product is a medicine that has not been approved. It may not be sold or used. The regulator also found fake samples.
  • The US FDA (2025) sent warning letters to five online sellers. It called Lemon Bottle an unapproved new drug. That is because the law treats a product sold to dissolve fat as a drug.
  • The UK pharmacy regulator (2025) warned pharmacists about supplying or injecting it.

No statement just about Lemon Bottle was found from the UK drug regulator (MHRA) or Australia’s drug regulator (TGA).

United States: FDA held that claims such as “LEMONBOTTLE LIPOLYSIS” and “non-surgical alternative to liposuction” establish intended use to affect the structure or function of the body, making the product a drug under section 201(g)(1) and, with no approved application, an unapproved new drug under sections 505(a) and 301(d). By contrast, deoxycholic acid injection (Kybella, NDA 206333, approved 2015-04-29) is labelled only for moderate to severe submental fullness in adults. Its approval rested on two randomised, double-blind, placebo-controlled trials (1,022 subjects) with at least 2-grade composite responses of 13.4% versus under 0.1% and 18.6% versus 3.0% on placebo, and its label warns of marginal mandibular nerve injury, dysphagia and injection-site ulceration and necrosis. FDA’s consumer page calls Kybella the only FDA-approved fat-dissolving injectable.

Switzerland: the cross-agency Expert Panel for Delimitation Questions classified the injected product as a medicinal product; a June 2024 addendum maintained this despite cosmetic labelling.

Compounding: the 503A framework concerns bulk ingredients, not finished imported products, so status is recorded as unknown.

Dose

Doses reported in trials and studies

How dosing worked in the studies

No trial has tested Lemon Bottle. These studies injected phosphatidylcholine (from lecithin) in other formulas. In the Reeds study, everyone knew what they got. 13 women signed up and 7 finished. One side of the lower belly was injected under the skin. The other side was left alone. They had 2 to 4 sessions, 8 weeks apart, with no more than 2500 mg phosphatidylcholine per session. In the Lee phase 1 trial, 26 healthy adults were assigned by chance to one dose. They got 250 mg or 500 mg of AYP-101, or a dummy treatment (placebo), under the skin below the chin. In the Choi phase II trial, 96 Asian adults were assigned by chance to AYP-101 at 25 mg/mL or 50 mg/mL, or placebo. They got shots every 2 weeks for up to 6 sessions.

Doses used in the studies are in the Scientific view.

Study doses are not personal dosing instructions. Reading doses safely: how concentration and syringe markings work.

Doses reported in studies, exactly as the cited trial reported them. They are not personal dosing instructions. Population, route and schedule matter more than the number.

No registered clinical trials are catalogued for this compound. The doses below come from other published studies in people.

Doses in other published studies

Published studies not listed in the trials table above: smaller or unregistered human studies first, then animal and cell studies. Doses are shown exactly as each study reported them. Animal studies report weight-based doses, absolute amounts or concentrations; none translates directly to people, and none is converted here.

SubjectsDesignDoseFindingSource
Humans: 13 women with BMI of 30 or less and lower-abdominal fat enrolled, 7 completed. Ingredient: Lecithin (phosphatidylcholine derived from soybean lecithins, given with sodium deoxycholate)Randomised, open-label study. One side of the lower abdomen below the umbilicus was injected; the other side was left untreated as the control.Each mL contained 50 mg phosphatidylcholine, 42 mg sodium deoxycholate and 8 mg benzyl alcohol. Injected into the lower-abdominal subcutaneous fat on one side, 2 to 4 sessions spaced 8 weeks apart, with no more than 2500 mg phosphatidylcholine per session.Anterior subcutaneous abdominal fat thickness fell significantly on the treated side (P = .004). Adipose tissue showed rapid increases in crown-like structures and macrophage infiltration, which the authors attributed to adipocyte necrosis, and plasma C-reactive protein, lipid profile and glucose were unchanged.Reeds DN et al., Aesthet Surg J, 2013
Humans: 9 healthy women with grade II-III thigh cellulite. Ingredient: Lecithin (phosphatidylcholine-based topical gel)Randomised, double-blinded split-thigh study: active gel on one thigh and placebo gel on the other. Both thighs also received LED light.Gel applied to the skin twice daily for 3 months. Each thigh also had a 15-minute red (660 nm) and near-infrared (950 nm) LED exposure twice weekly, 24 treatments in total. The abstract does not state the gel's concentration.At 3 months, 8 of 9 thighs treated with active gel plus LED were downgraded to a lower cellulite grade, while minimal clinical change was seen in the 9 placebo-gel thighs and the one non-responding active thigh. At 18 months, 5 of the 8 responding thighs had reverted to their original grade.Sasaki GH et al., J Cosmet Laser Ther, 2007
Humans: 26 healthy adults (22 men, 4 women). Ingredient: Lecithin (AYP-101, 93% soybean phosphatidylcholine made soluble with glycocholic acid, not deoxycholate)Randomised, double-blind, placebo-controlled, single-dose phase 1 trial in two cohorts (NCT05476094)One subcutaneous dose of 250 mg or 500 mg AYP-101, or placebo, given as 10 mL in total into submental fatAll 72 solicited adverse drug reactions (reported by 24 subjects, placebo group included) were mild, mostly injection-site pain and bruising, with no clinically significant difference in safety between groups. No clinically significant differences in pharmacokinetics or lipid profiles were seen between post-dose and baseline values in any dose group.Lee HJ et al., Lipids Health Dis, 2024
Humans: 96 Asian adults with moderate to severe submental fat. Ingredient: Lecithin (AYP-101, soybean phosphatidylcholine)Single-centre, randomised, double-blind, placebo-controlled phase II trialAYP-101 at 25 mg/mL or 50 mg/mL, or placebo, given as injections every 2 weeks for up to 6 sessions (the abstract does not state the volume per session)Four weeks after the final injection, at least a 1-grade improvement on the evaluator-rated scale (ER-SMFRS) was seen in 69.70% of the 25 mg/mL group, 48.39% of the 50 mg/mL group and 22.58% of the placebo group. The abstract reports a significant difference for 25 mg/mL versus placebo (P = 0.0002), with similar results at 12 weeks, and gives no P value for 50 mg/mL versus placebo.Choi SY et al., Clin Ther, 2025
Mice: 8-week-old male C57BL/6 mice on a 60%-fat diet. Ingredient: BromelainControlled animal study; mice randomly divided into bromelain and vehicle (PBS) groupsBromelain 20 mg/kg by oral gavage daily for 12 weeks, given alongside the high-fat dietCompared with vehicle, bromelain reduced diet-induced body weight gain by about 30%, white adipose tissue weight by about 40% and liver weight by about 20%, and lowered serum total cholesterol (about 15%) and triglycerides (about 25%). This was oral dosing, not injection into fat.Hu PA et al., Nutrients, 2020
Cells: human brown-like adipocytes made chemically from dermal fibroblasts, grown in vitamin-free, serum-free medium with choline. Ingredient: RiboflavinIn vitro concentration-response experimentsRiboflavin at 0.05 to 5 µg/mL in the culture medium throughout the experiments (the methods give a 3-week conversion period unless otherwise indicated)At 0.5 and 5 µg/mL riboflavin suppressed UCP1 and CIDEA expression (0.05 µg/mL slightly enhanced it), and at high concentrations it increased glycerol secretion, a lipolysis marker, while triglyceride storage fell slightly.Takeda Y et al., Sci Rep, 2024

How the blend's ratio compares with studied doses

No ratio of the declared ingredients (bromelain, lecithin and riboflavin, plus unnamed 'natural ingredients') appears on the packaging, in the marketing that regulators summarised, or in any published source found, so there is no fixed proportion to describe. If a pack did follow a fixed formula, any amount drawn from it would contain the ingredients in that proportion, but Swissmedic's 2024 laboratory testing found samples whose contents did not match the declared ingredients (one contained only caffeine). Neither bromelain nor riboflavin has any human evidence on fat reduction, and no human or animal study of either one injected into fat was found. Riboflavin has the least evidence here (the only fat-cell data found are from cell culture), and bromelain's fat-related data are a mouse cell-line study and oral dosing in mice on a high-fat diet, so these two ingredients limit what can be said about any amount of the mixture. Lecithin-derived phosphatidylcholine has been injected in human trials, but only at stated concentrations with a bile-acid solubiliser (deoxycholate or glycocholic acid), so those trials say nothing about the lecithin in this product. The evidence gives no safe or effective human dose or ratio for the blend, none of the ingredients provides a validated ceiling for injection into fat, and no study of the three ingredients together, in cells, animals or people, was found.

No controlled trial has tested this combination in people. The comparison uses each ingredient's own studies, which often differ in route and population, so it is not a dosing guide.

Doses reported in online communities (untested)

Unverified, and not a recommendation. These are amounts people describe in online forums such as Reddit, collected so researchers can see how practice differs from the evidence. These forum accounts are not clinical evidence, even where they overlap studied doses. Products sold online as "research peptides" are not FDA approved, and their identity, purity and strength are not verified; they can be mislabeled, contaminated or wrongly dosed.

What people report

In the threads reviewed (r/PlasticSurgery and r/30PlusSkinCare), posters described about 10 to 20 mL per treated area per session, on the double chin, jowls, lower cheeks and jaw, upper arms and abdomen, with sessions about a week apart. The main disagreement was whether it works at all: accounts split between visible reduction and no change, and one commenter said no scientific studies support it. Reported side effects were swelling, bruising, hard lumps and, in one account, swollen lymph nodes with dulled hearing; commenters also cited infections, abscesses and necrosis.

How this compares with the studies

Human studies of a related ingredient used phosphatidylcholine at stated concentrations (25 to 50 mg/mL, with deoxycholate or glycocholic acid), given once or at intervals of 2 to 8 weeks. The thread volumes are posters' own accounts of a product with no published formula and inconsistent contents in regulator testing, so they indicate no ingredient amount and cannot be compared with studied exposure, safety or efficacy.

Open questions a study would need to answer

Threads consulted, checked 2026-09-26: Lemon bottle fat dissolving (r/30PlusSkinCare) · Any success stories with lemon bottle fat dissolving injections? (r/PlasticSurgery) · Worth getting lemon bottle over normal fat dissolver? (r/PlasticSurgery) · Lemon bottle results (r/PlasticSurgery) · Hearing loss after lemon bottle (r/PlasticSurgery) · Lump after lemon bottle treatment (r/PlasticSurgery) · Lemon bottle - do you inject yourself? (r/30PlusSkinCare) · Lemon bottle Fat dissolving (r/30PlusSkinCare)

Enforcement history

Side effects and warnings

Full lists are in the .

Reported side effects

Interactions

Not catalogued yet.

Contraindications

Not catalogued yet.

Storage

Product characteristics

Form: Liquid solution in ampoules or vials; packaging reported by Swissmedic is labelled as a cosmetic product in German, French and Italian

Compound information

Declared ingredients on packaging and in marketing are mainly bromelain, lecithin and riboflavin plus unspecified natural ingredients; no quantitative formula has been published. Swissmedic's laboratory could not detect the declared ingredients in samples from various sources, so the contents of any given pack cannot be assumed from its label. No safety data sheet from a regulated drug manufacturer exists.

Molecule, patents, enforcement history, full trial tables and compound details are in the .

Common questions

What is Lemon Bottle?

Lemon Bottle is a brand of liquid made by SID Medicos. The company is in Seoul, South Korea. It is sold online and on social media as a "fat dissolving" liquid. Sellers also call it a "lipolysis" (fat breakdown) solution. Regulators in Switzerland, the United States and the UK all say it is being injected. But the company that sells it told regulators it is a cosmetic, meant only for use on the skin.

Is Lemon Bottle FDA approved?

Not FDA approved for any use.

What have studies found?

How was it dosed in studies?

No trial has tested Lemon Bottle. These studies injected phosphatidylcholine (from lecithin) in other formulas. In the Reeds study, everyone knew what they got. 13 women signed up and 7 finished. One side of the lower belly was injected under the skin. The other side was left alone. They had 2 to 4 sessions, 8 weeks apart, with no more than 2500 mg phosphatidylcholine per session. In the Lee phase 1 trial, 26 healthy adults were assigned by chance to one dose. They got 250 mg or 500 mg of AYP-101, or a dummy treatment (placebo), under the skin below the chin. In the Choi phase II trial, 96 Asian adults were assigned by chance to AYP-101 at 25 mg/mL or 50 mg/mL, or placebo. They got shots every 2 weeks for up to 6 sessions.

What are the side effects and warnings?

Is it legal to buy as a "research peptide"?

Products sold as "research use only" or "not for human consumption" are not approved for use in people. That label does not make them legal to sell for human use, and their contents are not checked by any regulator.

References

This page summarises the published sources below. PeptideBasics101 does no original research. Trial doses and results are reported as the cited study or label reported them. Sources can themselves be wrong or superseded; if you find a statement here that does not match its source, please tell us through our corrections process. Sources were last checked on 2026-09-23.

Based on 8 published references
  1. Swissmedic: warning about the illegal medicinal product Lemon Bottle lipolysis solution (2024, with June 2024 addendum) (swissmedic.ch)
  2. FDA warning letter 695821 (March 3, 2025): LemonBottle Ampoule Solution and other injectable lipolytic products as unapproved new drugs (fda.gov)
  3. FDA Roundup, March 11, 2025: six warning letters on unapproved fat-dissolving injectable drug products (fda.gov)
  4. FDA: using fat-dissolving injections that are not FDA approved can be harmful (fda.gov)
  5. General Pharmaceutical Council: GPhC highlights concerns about supply of unregulated products (April 2025) (pharmacyregulation.org)
  6. Kybella (deoxycholic acid) injection prescribing information (FDA label) (accessdata.fda.gov)
  7. Rotunda AM et al. Detergent effects of sodium deoxycholate are a major feature of an injectable phosphatidylcholine formulation used for localized fat dissolution. Dermatol Surg 2004 (pubmed.ncbi.nlm.nih.gov)
  8. Dave S et al. Inhibition of adipogenesis and induction of apoptosis and lipolysis by stem bromelain in 3T3-L1 adipocytes. PLoS One 2012 (pubmed.ncbi.nlm.nih.gov)

Clinical trial entries in the table above link to their ClinicalTrials.gov registry records. Spotted an error? See corrections.

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