Home › NDC Lookup › Ingredients › Salisylic Acid 1% › 73635-7102-05
Aftaseptic Instant Pain Relief Salisylic Acid 1% 10 mg/mL Liquid, 1 bottle — NDC 73635-7102-05 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Aftaseptic Instant Pain Relief Salisylic Acid 1% 10 mg/mL Liquid, 1 bottle — NDC 73635-7102-5 (Billing 73635-7102-05)

by Germa Products, LLC · 1 BOTTLE, WITH APPLICATOR in 1 BOX / 14.8 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of 1 bottle of Aftaseptic Instant Pain Relief Salisylic Acid 1% 10 mg/mL Liquid from Germa Products, LLC, marketed since Mar 2019 and currently FDA-listed. It is this product's only package size.

NDC 73635-7102-05
🏷️ FDA NDC (as labeled) 73635-7102-5 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 73635-7102-5
Product NDC 73635-7102
11-digit billing NDC 73635710205
RxCUI 1047362
UNII O414PZ4LPZ
UPC 0790933102055
Application # M022
SPL Set ID beb32fba-503a-f5e5-e053-2a95a90a57e5
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-03-29
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 1047362
Why two NDCs? The FDA registers this code as 73635-7102-5 — 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 → 73635-7102-05. 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.

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 is used in a facial routine for acne-prone and oil-prone skin. The routine includes a cleanser, serum, toner and emulsion. Salicylic acid helps loosen and shed dead skin cells.
  • Use the cleanser morning and evening, and the serum in the morning after cleansing. Use the toner in the evening on dry skin, and the emulsion at night after cleansing. Avoid your...
  • Mild stinging, burning, itching, dryness and extra peeling can happen. If dryness or peeling bothers you, try using the serum or toner every other day. If it gets excessive, stop a...
  • It is best not to. Using another topical acne medication at the same time makes irritation and dryness more likely. If you get irritated, use only one at a time.
📖 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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
73635-7102-05 You're viewing this Main listing 1 BOTTLE, WITH APPLICATOR in 1 BOX / 14.8 mL in 1 BOTTLE, WITH APPLICATOR 2019-03-29 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
ARTISTRY STUDiO Rose All Day Anti Acne Toner Pore Refresher 10 mg/mL 10056-0410-00 Access 200 ml — — FDA listed —
Biore 1 g/100g 10596-0199-05 Kao 1 tube — — FDA listed —
NAS Toner 1 g/1001 26052-0042-01 BURT'S 145 liquids — — FDA listed —
Clarifying Toner 1 g/100g 62742-4240-01 Allure 120 g — — FDA listed —
Biome-Balancing Clear and Prevent Acne (Blemish) Treatment Serum 1 g/100mL 70381-0134-02 Murad, 1 bottle — — FDA listed —
Aftaseptic Instant Pain Relief 10 mg/mLthis 73635-7102-05 Germa 1 bottle — — FDA listed —
Dr. C. Tuna Acne Blemish Control Serum 10 mg/mL 74690-0011-01 Farmasi 1 bottle — — FDA listed —
YOUR Anti Acne Serum .2 g/20mL 84229-0016-00 Skin 20 ml — — Discontinued —
Your Anti-Acne Serum .2 g/20mL 84229-2101-03 Skin 1 ml — — FDA listed —
Wart Remover 1 g/100mL 84302-0001-01 Shenzhen 30 ml — — Discontinued —
Sylvirene Milia Remover 1 g/100mL 85248-0071-01 Jiangxi 40 ml — — FDA listed —
Beilloso FACIAL BUMP REFINING ESSENCE 1 g/100mL 85248-0077-01 Jiangxi 30 ml — — FDA listed —
Serynth Milia Remover 1 g/100mL 85248-0107-01 Jiangxi 30 ml — — FDA listed —
Dermfree Milia Remover 1 g/100mL 85248-0125-01 Jiangxi 30 ml — — FDA listed —
Folupia Milia Remover 1 g/100mL 85248-0147-01 Jiangxi 30 ml — — FDA listed —
Flobow FACIAL BUMP REFINING ESSENCE 1 g/100mL 85248-0168-01 Jiangxi 30 ml — — FDA listed —
Lixuhya MILIA REMOVER ESSENCE 1 g/100mL 85248-0208-01 Jiangxi 40 ml — — FDA listed —
Butterflys tear MILIA REMOVER 1 g/100mL 85248-0213-01 Jiangxi 30 ml — — FDA listed —
Blemish Blitz Emergency Acne Serum .01 g/mL 85779-0003-01 Guangdong 20 ml — — FDA listed —
Milia remover .01 g/mL 87278-0006-01 Guangxi 30 ml — — FDA listed —
Xexlvov Milia Remover 1 g/100mL 87312-0147-01 Shanghai 30 ml — — FDA listed —
Byt Bangytong Milia Remover 1 g/100mL 87382-0107-01 Shenzhen 30 ml — — FDA listed —
Spesolskii Milia Remover Essence 1 g/100mL 87556-0001-01 BEST 30 ml — — FDA listed —
Asterose Wart Remover 1 g/100mL 87786-0003-01 Wenzhou 10 ml — — FDA listed —
Musizlee WART REMOVER 1 g/100mL 87786-0004-01 Wenzhou 10 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
Mar 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.

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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII G280W4MW6E
    Rhubarb is a plant extract used as a natural colorant and flavoring agent in medicines. It provides a distinctive color and taste to make the medication more appealing.

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

The official label also statesEthyl Alcohol, propylene glycol, purified water, rhubarb.

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.

Manufacturer & labeler

LabelerGerma Products, LLC
FDA applicationM022 (OTC MONOGRAPH DRUG)
Labeler code73635
First marketedMar 2019
Product typeHuman Otc Drug
Portfolio20 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.

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 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

for the temporary relief of pain associated with canker sores.

⏱️ Dosage and Administration 45 words ▾

Directions Use enclosed applicator brush Children 14 years of age to adult. Apply 2 brushstrokes 2 times a day to affected area of the mouth, gums or mucous membranes (throat). Do not rinse mouth after use. Children under 14 years of age consult a physician.

⚠️ Warnings 52 words ▾

Warnings Alcohol warning: if you consume 3 or more alcoholic drinks everyday, consult with a specialist whether you should use Salicylic Acid or other pain reliever, fever reducers n Salicylic Acid may cause stomach bleeding. Allergy alert: may cause a severe allergic reaction which may include: hives, facial swelling, asthma (wheezing), shock.

🧪 Active Ingredient 6 words ▾

Active Ingredient Salicylic Acid 1% w/v

🧪 Inactive Ingredients 9 words ▾

Inactive Ingredients Ethyl Alcohol, propylene glycol, purified water, rhubarb.

🎯 Purpose 2 words ▾

Purpose Analgesic

📄 When Using This Product 11 words ▾

Uses For the temporary relief of pain associated with canker sores.

📄 Keep Out of Reach of Children 85 words ▾

Warnings Flammable n Keep away from fire or flame. Do not use for teething or in children under 2 years of age When using this product n avoid contact with eyes. Do not use longer than 1 week unless directed by a doctor. If pregnant or nursing contact a Doctor before using. Stop use and ask a doctor if condition persists or worsen keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

📄 Other Information 32 words ▾

Other Information Store between 15º to 30ºC (59º to 86ºF). Cap bottle tightly. Do not accept if safety seal is broken or missing. Cap bottle tightly. Keep this box for future doubts.

📄 Package Label / Principal Display Panel 2 words ▾

Aftaseptic Aftaseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Germa Products, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Germa Products, LLC 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.
← 73635-7101-05 · Germa 73645-0001-01 · DONGYANG →
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.