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Acne Oil Control Primer Salicylic Acid 20 mg/g Liquid — NDC 62742-4211-02 package photo

Acne Oil Control Primer Salicylic Acid 20 mg/g Liquid

by Allure Labs · 1 TUBE in 1 CARTON (62742-4211-2) / 45 g in 1 TUBE (62742-4211-1)
NDC 62742-4211-02
🏷️ FDA NDC (as labeled) 62742-4211-2 billing pads the package 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) 62742-4211-2
Product NDC 62742-4211
11-digit billing NDC 62742421102
RxCUI 251577
UNII O414PZ4LPZ
Application # M006
SPL Set ID db9b5de2-c07c-0b21-e053-2995a90ae9a9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-04-01
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 62742-4211-2 — a 5-4-1 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 package segment → 62742-4211-02. 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

LabelerAllure Labs
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code62742
First marketedApr 2022
Product typeHuman Otc Drug
Portfolio72 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

📗 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 F01RIY4371
    A synthetic polymer made from acrylic compounds and taurate, this substance acts as a thickener and stabilizer. It helps give liquid medicines a smooth texture and keeps ingredients from separating.
  • UNII H70115MP4A
    A natural plant extract from Annickia chlorantha bark used as a flavoring agent and preservative in medicines. It may help mask bitter tastes and extend shelf life.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII UF7620L1W6
    A synthetic silicone polymer that acts as a thickener and absorbent in medicines. It helps create the right texture, improves how the product feels on skin or in the mouth, and can absorb excess moisture or oil in formulations.
  • UNII ZAD9OKH9JC
    An omega-3 fatty acid derived from marine sources or algae. It's included as a nutritional ingredient and helps stabilize the formulation's structure and consistency.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • UNII AAN7QOV9EA
    Icosapent is a purified omega-3 fatty acid derived from fish oil. It's included in some medicines as an active therapeutic ingredient rather than an inactive excipient, used to help manage certain lipid levels in the body.
  • UNII 9KJL21T0QJ
    Linoleic acid is an omega-6 fatty acid derived from plant oils. It serves as an emulsifier and skin conditioning agent in topical formulations, helping ingredients mix smoothly and improving product texture.
  • UNII 0RBV727H71
    A natural fatty acid derived from plant oils. It helps dissolve other ingredients and improve how the medicine spreads or absorbs in the body.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII CS4U38E731
    A plant-derived oil from nigella sativa seeds, used as a carrier and emollient in formulations. It helps dissolve or suspend active ingredients and improves product texture and absorption.
  • UNII 6SMK8R7TGJ
    Oleanolic acid is a natural plant compound used in medicines as a binder and thickening agent. It helps hold tablet ingredients together and can improve how the body absorbs the active drug.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII J7WWH9M8QS
    A plant-derived powder made from saw palmetto berries. It's included in some formulations as a natural ingredient and potential filler, though its primary role is typically as an active botanical rather than a structural excipient.
  • UNII 7J95K7ID2S
    A plant extract from the roots of Chinese skullcap, used as a natural coloring agent and to add mild flavor to medicines. It may also help preserve the product's stability.
  • UNII 836SJG51DR
    Sodium ascorbyl phosphate is a derivative of vitamin C that acts as an antioxidant and preservative in medications. It helps protect the drug's active ingredients from degradation caused by air and light exposure.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 22ADO53M6F
    A mineral salt derived from phosphoric acid, used as a buffer to maintain the pH balance of the medication and help stabilize the active ingredients.
  • UNII 3980JIH2SW
    A salt form of phosphoric acid that acts as a buffer and pH adjuster in medicines. It helps keep the product at the correct acidity level for stability and effectiveness.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • 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 U6WSN5SQ1Z
    Zinc gluconate is a form of zinc, a mineral, combined with gluconic acid. It's used as a supplement ingredient to provide zinc content in the formulation.

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

The official label also statesInactive Ingredients Water (Aqua), Dimethicone, Butylene Glycol, Dimethicone Crosspolymer, Ammonium Polyacryloyldimethyl Taurate, Hydroxyethylcellulose, Serenoa Serrulata (Saw Palmetto) Fruit Extract, Sodium Ascorbyl Phosphate, Niacinamide, Linoleic Acid, Linolenic Acid, Docosahexaenoic Acid, Eicosapentaenoic Acid, Nigella Sativa (Black Cumin) Seed Oil, Scutellaria Baicalensis Root Extract, Zinc Gluconate, Glycerin, Tocopherol, Oleanolic Acid, Enantia Chlorantha Bark Extract, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Disodium Phosphate, Phenoxyethanol, Polysorbate 60, Sodium Hydroxide, Sodium Phosphate.

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
PanOxyl Clarifying Exfoliant 2 g/100mL 00316-0296-04 Crown 118 ml — — FDA listed —
Hero Pore Release Blackhead Clearing 20 mg/mL 10237-0001-00 Church 100 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 —
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 Double Action Acne Serum 20 mg/mL 49967-0062-01 L'Oreal 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 —
Dr. Gross AB Acne Daily Breakout 20 mg/mL 51326-0179-01 Topiderm, 1 bottle — — FDA listed —
Clear Proof Blemish Control Toner Acne Medication 2 g/100mL 51531-6743-05 Mary 1 bottle — — FDA listed —
Anti-Everything Face Serum 2 g/100mL 54111-0180-01 Bentley 1 bottle — — FDA listed —
Emuaid 2 g/100mL 55926-0029-01 Speer 30 ml — — 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 —
Acne Warrior Clearing Astringent 2 g/100mL 61197-0121-00 Pacifica 236 ml — — FDA listed —
Clenziderm Pore Therapy Acne Treatment 20 mg/mL 62032-0612-04 Obagi 148 ml — — FDA listed —
Acne Oil Control Primer 20 mg/gthis 62742-4211-02 Allure 1 tube — — FDA listed —
Shea Moisture 2 g/100mL 64942-2355-02 Conopco 1 bottle — — FDA listed —
Jack Black Bump Fix 20 g/1000g 66738-0022-01 Jack 183 g — — FDA listed —
Pharma Clear Spot Treatment 2 g/100mL 67879-0104-51 PHARMAGEL 1 tube — — FDA listed —
AGE Bright Clearing Serum 20 mg/mL 68479-0184-00 Dermalogica, 3 ml — — FDA listed —
Breakout Clearing Booster 2 mg/100mL 68479-0772-00 Dermalogica, 2 ml — — FDA listed —
Breakout Clearing Booster 2 g/100mL 68479-0773-02 Dermalogica, 1 bottle — — FDA listed —
Neutrogena Clear Pore Oil-Eliminating Astringent 20 mg/mL 69968-0028-08 Kenvue 236 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 Stress Control Triple Action Toner 20 mg/mL 69968-0521-08 Kenvue 237 ml — — FDA listed —
Clean and Clear Essentials Acne Toner 20 mg/mL 69968-0820-08 Kenvue 240 ml — — FDA listed —
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0925-08 Kenvue 236 ml — — FDA listed —
Acne Spot Treatment 20 mg/mL 70060-1505-01 CosMedical 9 ml — — FDA listed —
e.l.f Plz Clarify Facial Oil 2 g/100mL 70412-0401-01 Zhejiang 30 ml — — FDA listed —
Exfo Tonic Acne Treatment 2 g/100mL 70764-0104-51 CONTROL 1 bottle — — FDA listed —
L BRI Pure n Natural Deep Clean Toner 20 mg/mL 71238-0218-00 L'BRI 188 ml — — FDA listed —
Viaderma Clear Acne Treatment 20 mg/mL 71262-0017-15 VIADERMA 1 bottle — — FDA listed —
Detox Drops Acne Toner 2 g/100mL 71499-0523-01 KENDO 1 bottle — — FDA listed —
FHF Day Breakthru 2 g/100g 72788-0142-11 Summer 1 bottle — — FDA listed —
Dr Throwers Oily Skin Facial Astringent 2 g/100g 72839-0611-02 Derma 57 g — — FDA listed —
Pore Refining Toner 2 g/100g 72957-0013-01 Private 195 g — — FDA listed —
Sunday Riley Peacekeeper Acne Treatment Serum 20 mg/mL 73001-0505-01 Sunday 1 pouch — — FDA listed —
Naturium Salicylic Acid Serum 2% 20 mg/mL 76354-0122-01 e.l.f. 1 bottle — — FDA listed —
e.l.f. PLZ Clarify Facial Oil 20 mg/mL 76354-0419-01 e.l.f. 1 bottle — — FDA listed —
The Inkey List 360 Acne Clearing Serum 20 mg/mL 81136-0028-01 Brand 1 bottle — — FDA listed —
Mara Clear Skin Mineral Milk Acne Treatment 20 mg/mL 81461-0002-00 Mara 30 ml — — FDA listed —
Dermeleve Scalp Psoriasis Treatment 2 g/100mL 81507-0006-01 Advanced 1 bottle — — FDA listed —
Peach and Lily Peaches Slices Acne Exfoliating toner 20 mg/mL 81515-0501-01 Peach 120 ml — — FDA listed —
Skinlycious Glow Exfoliant 2 g/100mL 81574-0001-01 Skinlycious 28 ml — — FDA listed —
CeraVe Developed with Dermatologists BHA Exfoliating Toner Acne Treatment 20 mg/mL 82046-0291-01 L'Oreal 237 ml — — FDA listed —
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 82046-0955-01 LOreal 1 bottle — — FDA listed —
Clarifying Toner 2 g/100mL 83286-0012-01 Drmtlgy, 189 ml — — FDA listed —
Bubble Super Clear Blemish Prevention Serum 20 mg/mL 83509-0001-01 BUBBLE 1 bottle — — FDA listed —
Doing The Work Salicylic Acid Acne Treatment 20 mg/mL 84234-0001-00 Personal 1 bottle — — FDA listed —
Personal Day Doing the Work Daily Exfoliating Treatment 20 mg/mL 84234-0002-00 Personal 1 bottle — — FDA listed —
Perricone MD Acne Relief Gentle Exfoliating Toner Salicylic Acid Acne Treatment 2 g/100mL 84448-0602-18 THG 1 bottle — — FDA listed —
AHA BHA Blemish Control and Exfoliating Serum 2 g/100mL 85439-0101-01 Banuskin, 30 ml — — FDA listed —
PHOFAY Salicylic Acid Acne Treatment Essence 20 mg/mL 87080-0001-00 Hangzhou 1 bottle — — FDA listed —
Walgreens Apricot Scrub Acne Treatment 20 mg/g 00363-0951-15 WALGREEN 170 g — — FDA listed —
Signature Care Blemish And Blackhead Control 20 mg/g 21130-0720-12 SAFEWAY, 227 g — — FDA listed —
Universal Clarifying Pad 20 mg/g 62742-4276-02 Allure 1 jar — — FDA listed —
Up and Up Blemish Controlling Apricot Scrub 20 mg/g 11673-0930-15 TARGET 170 g — — FDA listed —
DermaClear Pads 20 mg/g 62742-4076-02 Allure 1 jar — — 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

🏛️
2022
On the market since
Apr 2022
📍
2026
Currently FDA-listed
4 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 Salicylic Acid — the ingredient across all brands.

Top reported reactions

Dry Skin12,766
Erythema12,318
Acne11,763
Skin Burning Sensation11,557
Skin Irritation7,730
Skin Exfoliation5,759
Rash4,766

Age at onset

Neonate7
Infant1
Child16
Adolescent30
Adult334
Elderly131

Reporter sex

52,595 reports
Male · 27%
Female · 73%
Unknown · 0%

Serious outcomes

Hospitalization800
Death632
Life-threatening214
Disabling147
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 18,985 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
62742-4211-02 You're viewing this 1 TUBE in 1 CARTON (62742-4211-2) / 45 g in 1 TUBE (62742-4211-1) 2022-04-01 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 62742-4211-2, 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: 62742-4211-02, written without dashes as 62742421102. 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 62742-4211-02, the first segment (62742) is the labeler code FDA assigned to Allure Labs; the middle segment (4211) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Allure Labs. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Allure Labs 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 6 words ▾

Uses For the treatment of acne

⏱️ Dosage and Administration 69 words ▾

Directions Clean the skin thoroughly before applying this product Cover the entire affected area with a thin layer one to three times daily Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor If bothersome dryness or peeling occurs, reduce application to once a day or every other day

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 6 words ▾

Active Ingredients Salicylic Acid 2 %

🧪 Inactive Ingredients 65 words ▾

Inactive Ingredients Water (Aqua), Dimethicone, Butylene Glycol, Dimethicone Crosspolymer, Ammonium Polyacryloyldimethyl Taurate, Hydroxyethylcellulose, Serenoa Serrulata (Saw Palmetto) Fruit Extract, Sodium Ascorbyl Phosphate, Niacinamide, Linoleic Acid, Linolenic Acid, Docosahexaenoic Acid, Eicosapentaenoic Acid, Nigella Sativa (Black Cumin) Seed Oil, Scutellaria Baicalensis Root Extract, Zinc Gluconate, Glycerin, Tocopherol, Oleanolic Acid, Enantia Chlorantha Bark Extract, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Disodium Phosphate, Phenoxyethanol, Polysorbate 60, Sodium Hydroxide, Sodium Phosphate.

🎯 Purpose 3 words ▾

Purpose Acne Treatment

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 62742-4209-01 · Allure 62742-4212-02 · Allure →
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.