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Gly-Sal 10-2 Salicylic Acid 20 mg/mL Liquid, 89 mL — NDC 51326-0938-01 package photo

Gly-Sal 10-2 Salicylic Acid 20 mg/mL Liquid, 89 mL

by Topiderm, Inc. · 89 mL in 1 BOTTLE, PLASTIC (51326-938-01)
NDC 51326-0938-01
🏷️ FDA NDC (as labeled) 51326-938-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 51326-938-01
Product NDC 51326-938
11-digit billing NDC 51326093801
RxCUI 1048903
UNII O414PZ4LPZ
Application # M006
SPL Set ID 661cc58b-9360-4b96-b405-afdc2e378397
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-06-10
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 51326-938-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 51326-0938-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Salicylic acid and derivatives class.

Drug family (ATC) Salicylic acid and derivatives, Other antifungals for topical use, Antiinflammatory agents, non-steroids
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerTopiderm, Inc.
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code51326
First marketedJun 2019
Product typeHuman Otc Drug
Portfolio46 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

📖 What it is MedlinePlus · NLM

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or b...

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It's designed to treat acne. Salicylic acid helps by loosening and removing dead skin cells that clog pores — the buildup that leads to breakouts. The multi-step system on this lab...
  • What is this salicylic acid product actually supposed to do for my skin?
  • Some mild tingling, stinging, and peeling is actually expected — that's the salicylic acid doing its job by clearing away dead skin cells. But if the burning or peeling feels exces...
  • My skin feels like it's burning and peeling. Is that normal?
📖 Read our full Salicylic Acid Topical guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • 100 mg / 1 mL UNII 0WT12SX38S
    Glycolic acid is an alpha-hydroxy acid derived from sugar cane that helps dissolve and remove dead skin cells. In topical medicines, it works as an exfoliant and pH adjuster to improve skin penetration and product effectiveness.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII 5Q87K461JO
    A synthetic conditioning agent derived from linoleic acid and propylene glycol. It works as an antistatic agent and hair conditioner in topical formulations, helping reduce friction and improve product spreadability.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 353VA59XH8
    A synthetic surfactant derived from petroleum-based alcohols. It helps dissolve and mix oil and water components in liquid formulations, improving the medicine's consistency and how active ingredients distribute throughout the product.
  • UNII O9W3D3YF5U
    A synthetic surfactant derived from petroleum-based olefins. It helps dissolve or suspend active ingredients and other substances in liquid formulations, improving how the medicine mixes and flows.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII C32PQ86DH4
    Zinc PCA is a zinc salt of pyroglutamic acid, a naturally occurring amino acid derivative. It's used in medications as a skin-conditioning agent and to help maintain product stability and texture in topical formulations.

13 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAcetone, Ammonium Hydroxide, Disodium EDTA, Glycolic Acid, Hamamelis Virginiana (Witch Hazel) Water, Imidazolidinyl Urea, Polysorbate-20, Purified Water, SD Alcohol 40B (13% v/v) Sodium Benzoate

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Differin Acne Clearing Body 2 g/100g 00299-4132-00 Galderma 170 g — — FDA listed —
PanOxyl Acne Banishing Body (Spray) 2 g/100g 00316-0297-01 Crown 170 g — — FDA listed —
Ology Acne Clearing Body Mist 20 mg/mL 00363-9659-10 Walgreens 1 tube — — FDA listed —
Sulfur 8 Scalp Therapy Medicated Dandruff Control 20 mg/mL 12022-0032-00 J. 355 ml — — FDA listed —
Doo Gro Braids Twists Locs Dandruff Control Moisturizing 20 mg/mL 12022-0041-00 J. 335 ml — — FDA listed —
Topicals Clearly Mist 20 mg/mL 51326-0307-01 Topiderm, 1 bottle — — FDA listed —
Gly-Sal 10-2 20 mg/mLthis 51326-0938-01 Topiderm, 89 ml — — FDA listed —
Pacifica Bacne Warrior 2 g/100mg 61197-0103-00 Pacifica 177 mg — — FDA listed —
Neutrogena Stubborn Body Acne Treatment 20 mg/mL 69968-0758-06 Kenvue 162 ml — — FDA listed —
Tiege Hanley Acne All Over Body 2 g/100g 71714-0005-01 Tiege 1 canister — — FDA listed —
Acne Banishing Body 2 g/100g 72667-0218-06 Inspec 170 g — — Discontinued —
Body Acne Treatment 20 mg/g 73318-7007-03 Skin 1 bottle — — FDA listed —
Naturium Salicylic Acid Body 2% 20 mg/mL 76354-0124-01 e.l.f. 120 ml — — FDA listed —
e.l.f Skin Acne-Treating Body Mist 20 mg/mL 76354-0418-01 e.l.f. 1 bottle — — FDA listed —
Bha Toner 2 g/100mL 83286-0018-01 Drmtlgy, 189 ml — — FDA listed —
PAPATUI Acne Fighting Body 2 g/100g 83850-0200-00 PAPATUI, 170 g — — FDA listed —
First Aid Beauty Body Acne Clearing Mist 2 g/100mL 84126-0120-88 The 1 bottle — — FDA listed —
Saltair Acne Bodyspray 2 g/100g 87290-0003-04 Saltair 1 bottle — — FDA listed —
Kugig Acne Treatment Sprayer 2 g/100mL 87722-0001-01 Guangdong 100 ml — — FDA listed —
Skin Pharmacy Advanced Acne Therapy Clarifying Daily Cleanser 20 mg/mL 69842-0064-01 CVS 148 ml — — FDA listed —
Skinpharmacy Advanced Acne Therapy Overnight Salicylic Acid 20 mg/mL 69842-0066-01 CVS 1 tube — — FDA listed —
SKIN MEDICA Purifying Foaming Wash 20 mg/mL 00023-4948-05 Allergan, 1 bottle — — FDA listed —
Differin Acne Clearing Body Scrub 20 mg/mL 00299-4609-00 Galderma 237 ml — — FDA listed —
Sulfur 8 Anti-Dandruff Braid 20 mg/mL 12022-0021-00 J. 356 ml — — FDA listed —
Sulfur 8 Fresh Anti-Dandruff 20 mg/mL 12022-0028-00 J. 355 ml — — FDA listed —
Sulfur 8 Medicated Dandruff with Salicylic Acid 20 mg/mL 12022-0039-00 J. 222 ml — — FDA listed —
Glovers Therapeutic Care 20 mg/mL 12022-0040-00 J. 118 ml — — FDA listed —
Signature Care Acne Treatment 20 mg/mL 21130-0722-77 SAFEWAY, 177 ml — — FDA listed —
Kiehls Since 1851 Dermatologist Solutions Truly Targeted Acne Clearing Solution 20 mg/mL 49967-0055-01 L'Oreal 1 bottle — — FDA listed —
Thayers Since 1847 Natural Remedies Blemish Clearing Witch Hazel Aloe Vera Formula Pads 20 mg/mL 49967-0705-01 L'Oreal 60 applicators — — FDA listed —
Dr. Gross AB Acne Daily Breakout 20 mg/mL 51326-0179-01 Topiderm, 1 bottle — — FDA listed —
Replenix Acne Gly-Sal 2-2 Foaming Cleanser 20 mg/mL 51326-0929-06 Topiderm, 200 ml — — FDA listed —
Medicated Wash 20 mg/mL 67226-1021-01 Vivier 150 ml — — FDA listed —
L BRI Pure n Natural Deep Clean Toner 20 mg/mL 71238-0218-00 L'BRI 188 ml — — FDA listed —
Peach and Lily Peaches Slices Acne Exfoliating toner 20 mg/mL 81515-0501-01 Peach 120 ml — — FDA listed —
Doing The Work Salicylic Acid Acne Treatment 20 mg/mL 84234-0001-00 Personal 1 bottle — — FDA listed —
Byoma Acne Clearing Cleanser 20 mg/mL 84821-0007-01 Byoma 175 ml — — FDA listed —
PHOFAY Salicylic Acid Acne Treatment Essence 20 mg/mL 87080-0001-00 Hangzhou 1 bottle — — FDA listed —
Hero Pore Release Blackhead Clearing 20 mg/mL 10237-0001-00 Church 100 ml — — FDA listed —
Up and Up Acne Wash 20 mg/mL 11673-0024-54 TARGET 269.1 ml — — FDA listed —
Gly-Sal 5-2 20 mg/mL 51326-0927-01 Topiderm, 200 ml — — FDA listed —
Clean and Clear Essentials Acne Toner 20 mg/mL 69968-0820-08 Kenvue 240 ml — — FDA listed —
Viaderma Clear Acne Treatment 20 mg/mL 71262-0017-15 VIADERMA 1 bottle — — FDA listed —
Naturium Salicylic Acid Serum 2% 20 mg/mL 76354-0122-01 e.l.f. 1 bottle — — FDA listed —
OXY Volcanic Ash Acne Face Wash 20 mg/mL 10742-8334-01 The 207 ml — — FDA listed —
Clean and Clear Essentials Deep Cleaning Astringent 20 mg/mL 69968-0209-08 Kenvue 240 ml — — FDA listed —
Neutrogena Oil Free Acne Wash 20 mg/mL 69968-0675-01 Kenvue 12 tubes — — Discontinued —
Neutrogena Oil Free Acne Wash 20 mg/mL 69968-0770-01 Kenvue 12 tubes — — Discontinued —
CeraVe Developed with Dermatologists BHA Exfoliating Toner Acne Treatment 20 mg/mL 82046-0291-01 L'Oreal 237 ml — — FDA listed —
Byoma Acne Clearing Body Wash 20 mg/mL 84821-0005-01 Byoma 400 ml — — FDA listed —
Nativae Milia Acne Serum 20 mg/mL 85065-0557-00 CDE 30 ml — — FDA listed —
pHisoderm Clear Confidence Daily Gel Face Wash 20 mg/mL 10742-1412-01 The 177 ml — — FDA listed —
Thayers Since 1847 Natural Remedies Double Action Acne Serum 20 mg/mL 49967-0062-01 L'Oreal 1 bottle — — FDA listed —
Exuviance Daily Acne Peel 20 mg/mL 58414-0017-02 NeoStrata 1 bottle — — FDA listed —
Atrix Clarifying Toner 20 mg/mL 59088-0444-08 PureTek 118 ml — — FDA listed —
Neutrogena Clear Pore Oil-Eliminating Astringent 20 mg/mL 69968-0028-08 Kenvue 236 ml — — FDA listed —
Sunday Riley Peacekeeper Acne Treatment Serum 20 mg/mL 73001-0505-01 Sunday 1 pouch — — FDA listed —
Replenix Gly-Sal 10-2 cleanser 20 mg/mL 51326-0928-01 Topiderm, 200 ml — — FDA listed —
Clenziderm Daily Care Foaming Cleanser Acne Treatment 20 mg/mL 62032-0610-11 Obagi 118 ml — — FDA listed —
Neutrogena Body Clear Body Wash Pink Grapefruit 20 mg/mL 69968-0910-09 Kenvue 250 ml — — FDA listed —
Amazon Basics Acne Wash Acne treatment 20 mg/mL 72288-0955-01 AMAZON.COM 177 ml — — FDA listed —
e.l.f. PLZ Clarify Facial Oil 20 mg/mL 76354-0419-01 e.l.f. 1 bottle — — FDA listed —
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 82046-0955-01 LOreal 1 bottle — — FDA listed —
Personal Day Doing the Work Daily Exfoliating Treatment 20 mg/mL 84234-0002-00 Personal 1 bottle — — FDA listed —
Thayers Since 1847 Natural Remedies Blemish Clearing Witch Hazel Aloe Vera Formula Toner 20 mg/mL 49967-0523-01 L'Oreal 355 ml — — FDA listed —
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 51150-0995-01 SICOS 1 bottle — — FDA listed —
Clenziderm Pore Therapy Acne Treatment 20 mg/mL 62032-0612-04 Obagi 148 ml — — FDA listed —
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0521-08 Kenvue 237 ml — — FDA listed —
Acne Control Cleanser 20 mg/mL 79903-0339-12 Walmart 355 ml — — FDA listed —
Target Up and Up Salicylic Acid Acne Wash 20 mg/mL 82442-0014-87 TARGET 236.5 ml — — FDA listed —
Replenix Gly-Sal 2-2 20 mg/mL 51326-0925-01 Topiderm, 200 ml — — FDA listed —
Neutrogena Oil-Free Acne Wash Sensitive Skin Facial Cleanser Fragrance Free 20 mg/mL 69968-0889-01 Kenvue 14 ml — — FDA listed —
Neutrogena Oil-Free Acne Wash Daily Scrub 20 mg/mL 69968-0908-04 Kenvue 124 ml — — FDA listed —
Neutrogena Oil-Free Acne Stress Control Power Clear Scrub 20 mg/mL 69968-0909-04 Kenvue 125 ml — — FDA listed —
The Inkey List 360 Acne Clearing Serum 20 mg/mL 81136-0028-01 Brand 1 bottle — — FDA listed —
Acne Wash 20 mg/mL 63940-0053-54 Harmon 269 ml — — FDA listed —
AGE Bright Clearing Serum 20 mg/mL 68479-0184-00 Dermalogica, 3 ml — — FDA listed —
Clean and Clear Acne Exfoliating Cleanser 20 mg/mL 69968-0822-05 Kenvue 148 ml — — FDA listed —
Neutrogena Oil Free Acne Wash Pink Grapefruit Facial Cleanser 20 mg/mL 69968-0926-06 Kenvue 177 ml — — FDA listed —
Neutrogena Evenly Clear Acne Cleanser 20 mg/mL 69968-0942-01 Kenvue 12 tubes — — FDA listed —
pHisoderm Clear Confidence Body Wash 20 mg/mL 10742-1442-01 The 295 ml — — FDA listed —
Phisoderm Anti Blemish Body Wash 20 mg/mL 10742-8451-01 The 295 ml — — FDA listed —
Neutrogena Oil Free Acne Wash Pink Grapefruit Facial Cleanser 20 mg/mL 69968-0686-06 Kenvue 177 ml — — FDA listed —
Salicylic acid 20 mg/mL 76162-0414-32 Topco 355 ml — — FDA listed —
Bubble Super Clear Blemish Prevention Serum 20 mg/mL 83509-0001-01 BUBBLE 1 bottle — — FDA listed —
Satinique Anti Dandruff Scalp and Hair 20 mg/mL 10056-0536-00 Access 280 ml — — FDA listed —
Kroger Clarify Care Acne Wash 20 mg/mL 30142-0945-77 THE 177 ml — — FDA listed —
Neutrogena All in 1 Acne Control Daily Scrub 20 mg/mL 69968-0092-04 Kenvue 124 ml — — FDA listed —
Neutrogena Body Clear Body Wash 20 mg/mL 69968-0655-09 Kenvue 250 ml — — FDA listed —
Neutrogena Oil-Free Acne Wash Pink Grapefruit Foaming Scrub 20 mg/mL 69968-0912-02 Kenvue 59 ml — — FDA listed —
Mara Clear Skin Mineral Milk Acne Treatment 20 mg/mL 81461-0002-00 Mara 30 ml — — FDA listed —
Atrix Antibacterial Wash 20 mg/mL 59088-0445-08 PURETEK 118 ml — — FDA listed —
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0925-08 Kenvue 236 ml — — FDA listed —
L BRI Deep Clean Toner 20 mg/mL 71238-0921-00 L'BRI 177 ml — — FDA listed —
Acne Control Cleanser 20 mg/mL 51316-0893-01 CVS 237 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2019
On the market since
Jun 2019
📍
2026
Currently FDA-listed
7 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Salicylic Acid (matched by generic name) — the program that covers self-administered drugs. 2 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Salicylic Acid. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$11.2K
Claims incl. refills
43
Beneficiaries
35
Spend / beneficiary
$319.01
Spend / claim
$259.66
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Gly-Sal 10-2 (this brand).

Top reported reactions

Vomiting216
Pruritus205
Weight Decreased188
Condition Aggravated184
Urticaria184
Weight Increased183
Hypertension181

Reporter sex

1,853 reports

Serious outcomes

Death611
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 128 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
51326-0938-01 You're viewing this 89 mL in 1 BOTTLE, PLASTIC (51326-938-01) 2019-06-10 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 51326-938-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 51326-0938-01, written without dashes as 51326093801. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 51326-0938-01, the first segment (51326) is the labeler code FDA assigned to Topiderm, Inc.; the middle segment (0938) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Topiderm, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Topiderm, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 17 words ▾

Uses For the treatment of acne of the body, with the skin enhancement properties of glycolic acid

⏱️ Dosage and Administration 60 words ▾

Directions Spray the entire affected area of the body one to three times daily. Because excessive drying of the skin can occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a physician. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

⚠️ Warnings 113 words ▾

Warnings For external use only. Direct spray away from face, especially eyes, lips and mouth. If irritation develops, discontinue use and consult a doctor.

Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Keep out of reach of children.

If swallowed, seek professional assistance or contact a Poison Control Center immediately. Flammable; keep tightly closed, away from flame and heat. Sunscreen use is recommended with any Glycolic Acid product and for an additional week thereafter, because some individuals may be more sensitive to sunlight.

🧪 Active Ingredient 5 words ▾

Active ingredient Salicylic Acid 2%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients Acetone, Ammonium Hydroxide, Disodium EDTA, Glycolic Acid, Hamamelis Virginiana (Witch Hazel) Water, Imidazolidinyl Urea, Polysorbate-20, Purified Water, SD Alcohol 40B (13% v/v) Sodium Benzoate

🎯 Purpose 3 words ▾

Purpose Acne medication

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
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For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.