Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Acne Treatment Cotton Pads 2 g/100g Cloth, 100 g — NDC 84356-003-01 (Billing 84356-0003-01)
by Guangzhou Yapeng Refinement Chemical Co., Ltd. · 100 g in 1 BOX
This is a package of 100 g of Acne Treatment Cotton Pads 2 g/100g Cloth from Guangzhou Yapeng Refinement Chemical Co., Ltd., marketed since Jun 2025 and currently FDA-listed. It is this product's only package size.
NDC 84356-0003-01
🏷️ FDA NDC (as labeled)
84356-003-01
billing pads the product segment with a zero
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
84356-003-01
Product NDC
84356-003
11-digit billing NDC
84356000301
RxCUI
797892
UNII
O414PZ4LPZ
Application #
M006
SPL Set ID
37ad7cd7-92df-82d9-e063-6294a90a0f04
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2025-06-16
Route
TOPICAL
Dosage form
CLOTH
Substance
SALICYLIC ACID
Quick answers
- RxCUI (RxNorm): 797892
Why two NDCs?
The FDA registers this code as 84356-003-01 — 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 → 84356-0003-01. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
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.
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about ACNE TREATMENT COTTON PADS?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per each | Per 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 84356-0003-01 You're viewing this Main listing | 100 g in 1 BOX | 2025-06-16 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Stridex Maximum 2 g/100mL 10157-1006-01 | Blistex | 1 jar | — | — | FDA listed | — |
| Stridex XL Face and Body Pads 2 g/100mL 10157-2114-01 | Blistex | 1 jar | — | — | FDA listed | — |
| OXY ADVANCED CARE 3 in 1 RETEXTURIZING CLEANSING PADS 20 mg 10742-1000-01 | The | 90 swabs | — | — | FDA listed | — |
| Oxy Deep Pore Acne Cleansing Pads 20 mg 10742-1006-01 | The | 90 cloths | — | — | FDA listed | — |
| Oxy 3-IN-1 Acne Cleansing Pads 20 mg 10742-1008-01 | The | 90 cloths | — | — | FDA listed | — |
| Oxy 3-IN-1 Acne Cleansing Pads 20 mg 10742-1010-01 | The | 90 fors | — | — | FDA listed | — |
| Oxy Deep Pore Acne Cleansing Pads 20 mg 10742-1011-01 | The | 90 fors | — | — | FDA listed | — |
| OXY ADVANCED CARE MAXIMUM STRENGTH 3-in-1 ACNE PADS 20 mg 10742-1200-01 | The | 90 swabs | — | — | FDA listed | — |
| OXY Deep Pore Cleansing Pads 20 mg 10742-4204-01 | The | 90 swabs | — | — | FDA listed | — |
| OXY 3 in 1 Acne Pads 20 mg 10742-4359-01 | The | 90 swabs | — | — | FDA listed | — |
| Proactiv CLEAR ZONE BODY PADS 2 g/100mL 11410-0056-00 | Alchemee, | 75 applicators | — | — | FDA listed | — |
| ZO Skin Health Oil Control Pads Acne Treatment 20 mg/mL 42851-0085-30 | ZO | 30 patches | — | — | 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 | — |
| Gly-Sal 5-2 Pads .02 g 51326-0038-60 | Topiderm, | 60 cloths | — | — | FDA listed | — |
| Gly-Sal 10-2 Pads .02 g 51326-0039-60 | Topiderm, | 60 cloths | — | — | FDA listed | — |
| Gly-Sal 10-2 20 mg 51326-0712-60 | Topiderm, | 60 cloths | — | — | FDA listed | — |
| Gly-Sal 2-2 Pads 20 mg 51326-0923-01 | Topiderm, | 60 cloths | — | — | FDA listed | — |
| Max Complexion Correction Pads 2 g/100mL 54031-0501-22 | PETER | 60 patches | — | — | FDA listed | — |
| Equate Beauty Quick Action Pads Salicylic Acid Acne Treatment 20 mg/mL 61805-0117-01 | Bath | 90 patches | — | — | FDA listed | — |
| DermaClear Pads 20 mg/g 62742-4076-02 | Allure | 1 jar | — | — | FDA listed | — |
| Universal Clarifying Pad 20 mg/g 62742-4276-02 | Allure | 1 jar | — | — | FDA listed | — |
| Clearasil Rapid Rescue Deep Treatment Pads .02 g 63824-0431-90 | Reckitt | 90 cloths | — | — | FDA listed | — |
| Noxzema ANTIBLEMISH .02 g/g 64942-1259-01 | Conopco | 0284 g | — | — | FDA listed | — |
| Rush Salicylc Acid Complexion Pads 2 g/100g 65113-1201-01 | G.S. | 1 jar | — | — | FDA listed | — |
| Anti-Aging Blemish Control Peel Pads 2.366 g/118.29g 65278-0318-01 | June | 118.29 g | — | — | FDA listed | — |
| Neutrogena Rapid Clear Treatment Pads 20 mg 69968-0719-06 | Kenvue | 60 cloths | — | — | FDA listed | — |
| Retexturizing Body Pads 2 g/100mm 70381-0126-02 | Murad, | 1 jar | — | — | FDA listed | — |
| Cleansing Wipes 2 g/100mL 71613-0001-01 | Nextcell | 25 applicators | — | — | FDA listed | — |
| FHF Change Peel Pads 2 g/100g 72788-0183-02 | Summer | 1 bottle | — | — | FDA listed | — |
| Acne Correction Pads 2 g/100mL 72957-0012-01 | Private | 1 jar | — | — | FDA listed | — |
| AHA/BHA Swipes 2 g/100mL 73318-7004-06 | SKIN | 1 jar | — | — | FDA listed | — |
| ESSENCE BY CATHERINE HINDS PURIFYING PADS with 2% Salicylic Acid 2 g/100mL 76446-0022-50 | Anna | 1 jar | — | — | FDA listed | — |
| anna lotan PURIFYING PADS with 2% Salicylic Acid 2 g/100mL 76446-0039-50 | Anna | 1 jar | — | — | Discontinued | — |
| Equate 2% Salicylic acid Acne treatment pad 2 g/100g 79903-0062-01 | Walmart, | 165 g | — | — | FDA listed | — |
| Maximum Sterngth Cleansing Pads Equate 2 g 79903-0207-01 | Walmart | 1 jar | — | — | FDA listed | — |
| Tingl Exfoliating Pads 2 g/100g 83286-0011-01 | Drmtlgy, | 60 patches | — | — | FDA listed | — |
| Crystal Clear Acne Treatment Pads 2 g/100mL 83316-0001-01 | Skin | 60 patches | — | — | Discontinued | — |
| First Aid Beauty Acne Clearing Pads 2 g/100mL 84126-0119-60 | The | 60 patches | — | — | FDA listed | — |
| Tula Skincare Breakout Breakthrough Acne Toner Pads 2 g/1001 84126-0152-30 | The | 1 jar | — | — | FDA listed | — |
| Acne Treatment Cotton Pads 2 g/100gthis 84356-0003-01 | Guangzhou | 100 g | — | — | FDA listed | — |
| Societe Clear Skin Pads 2 g/100g 87700-0147-02 | Societe | 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2025
On the market since
Jun 2025
📍
2026
Currently FDA-listed
1 year 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.
- FDA Orange Book · refreshed Oct 3, 2026
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 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 F2VW3D43YT
Azelaic acid is a naturally occurring compound that acts as a preservative and antimicrobial agent in medications. It helps prevent bacterial and fungal growth, extending the product's shelf life and stability.
-
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 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 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 WV9CM0O67Z
Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
-
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 YSE9PPT4TH
Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
8 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesAqua (Water), Niacinamide, Butylene Glycol, Ethylhexylglycerin, Azelaic Acid, Hamamelis Virginiana (Witch Hazel)Extract, Sodium Hyaluronate, Panthenol, Acrylates Copolymer, Phenoxyethanol
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerGuangzhou Yapeng Refinement Chemical Co., Ltd.
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code84356
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio7 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 openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Use ■ Treats acne and prevents breakouts ■ Removes blackheads and minimizes pores ■ Gently exfoliates dead skin cells ■ Improves skin texture and tone
⏱️ Dosage and Administration ▾
Directions ■ Cleanse and dry face thoroughly. ■ Gently wipe the pad over affected areas (avoid eye contour). ■ Use once daily (evening recommended) for normal skin, or every other day for sensitive skin. ■ Follow with moisturizer. For first-time users: Test on a small area before full application.
⚠️ Warnings ▾
Warnings Do not use on injured wounds
📦 Storage and Handling ▾
Other information ■ Storage: Keep container tightly closed at 15-25°C (59-77°F). . ■ Shelf Life: 24 months unopened; discard if pads dry out. ■ Eco-Friendly: Biodegradable cotton pads; recycle outer packaging.
🧪 Active Ingredient ▾
Active Ingredient(s) Salicylic Acid 2%
🧪 Inactive Ingredients ▾
Inactive ingredients Aqua (Water), Niacinamide, Butylene Glycol, Ethylhexylglycerin, Azelaic Acid, Hamamelis Virginiana (Witch Hazel)Extract, Sodium Hyaluronate, Panthenol, Acrylates Copolymer, Phenoxyethanol
🎯 Purpose ▾
Purpose Acne treatment
📄 Do Not Use ▾
Do not use ■ If allergic to salicylic acid or any ingredient. ■ On broken, sunburned, or irritated skin. ■ With other acne medications containing salicylic acid, unless directed by a doctor.
📄 When Using This Product ▾
■ Mild tingling or redness may occur initially (discontinue if severe). ■ Avoid sun exposure after use; apply sunscreen daily. ■ Do not combine with harsh scrubs or alcohol-based products. ■ Keep away from eyes and mucous membranes.
📄 Stop Use and Ask a Doctor If ▾
Severe irritation, rash, or peeling develops. No improvement after 12 weeks of regular use. Signs of allergic reaction (swelling, itching, dificulty breathing). .
📄 Keep Out of Reach of Children ▾
Contains salicylic acid; harmful if swallowed. If ingested, contact Poison Control immediately (U.S.: 1-800-222-1222).
📄 Package Label / Principal Display Panel ▾
Package Label - Principal Display Panel undefined
No label section mentions that — try another word, or open the full label on DailyMed below.
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 Guangzhou Yapeng Refinement Chemical Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Yapeng Refinement Chemical Co., Ltd. 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.
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.