Home › NDC Lookup › Ingredients › Zinc Oxide,Niacinamide,Colloidal Sulfur,... › 84509-0108-01
PEGO Acne Buster Salicylic Acid Drying Serum ZINC OXIDE,NIACINAMIDE,COLLOIDAL SULFUR,AZELAIC ACID,SALICYLIC ACID. .2 mg/10mL; .03 mg/10mL; .024 mg/10mL; .05 mg/10mL; .018 mg/10mL Liquid, 10 mL — NDC 84509-0108-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

PEGO Acne Buster Salicylic Acid Drying Serum ZINC OXIDE,NIACINAMIDE,COLLOIDAL SULFUR,AZELAIC ACID,SALICYLIC ACID. .2 mg/10mL; .03 mg/10mL; .024 mg/10mL; .05 mg/10mL; .018 mg/10mL Liquid, 10 mL — NDC 84509-108-01 (Billing 84509-0108-01)

by Guangzhou Senmai Biotechnology Co.,Ltd. · 10 mL in 1 BOTTLE

This is a package of 10 mL of PEGO Acne Buster Salicylic Acid Drying Serum ZINC OXIDE,NIACINAMIDE,COLLOIDAL SULFUR,AZELAIC ACID,SALICYLIC ACID. .2 mg/10mL; .03 mg/10mL; .024 mg/10mL; .05 mg/10mL; .018 mg/10mL Liquid from Guangzhou Senmai Biotechnology Co.,Ltd., marketed since May 2026 and currently FDA-listed. It is this product's only package size.

NDC 84509-0108-01
🏷️ FDA NDC (as labeled) 84509-108-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 27, 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

NDC database record

One package, one record: these facts belong to NDC 84509-108-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84509 labeler · 108 product · 01 package
Package marketed since
May 6, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8450910801 7
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84509-108-01
Product NDC 84509-108
11-digit billing NDC 84509010801
UNII SOI2LOH54Z, 70FD1KFU70, F2VW3D43YT, 25X51I8RD4, O414PZ4LPZ
Application # M016
SPL Set ID 511eaced-c4d8-ae94-e063-6394a90a320e
Physiologic effect Decreased Protein Synthesis; Decreased Sebaceous Gland Activity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-05-06
Route TOPICAL
Dosage form LIQUID
Substance ZINC OXIDE; SULFUR; AZELAIC ACID; NIACINAMIDE; SALICYLIC ACID
Why two NDCs? The FDA registers this code as 84509-108-01 — 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 → 84509-0108-01. 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.

Clinical

🧪 What is this product?

PEGO Acne Buster Salicylic Acid Drying Serum is a topical liquid marketed as an over-the-counter acne product under FDA monograph rules. It contains salicylic acid, which is typically used to exfoliate skin and unclog pores, along with azelaic acid and sulfur, both commonly used in acne formulations. Niacinamide and zinc oxide are included as skin-conditioning agents, with zinc oxide also functioning as a mild astringent. This product is meant to be applied to the skin as directed on the label.

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
84509-0108-01 You're viewing this Main listing 10 mL in 1 BOTTLE 2026-05-06 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PEGO Acne Buster Salicylic Acid Drying Serum .2 mg/10mL; .03 mg/10mL; .024 mg/10mL; .05 mg/10mL; .018 mg/10mLthis 84509-0108-01 Guangzhou 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

🏛️
2026
On the market since
May 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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 RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • 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 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 7E6SK9QDT8
    Cyclodextrins are ring-shaped sugar molecules derived from starch. They're used in medicines as solubilizers to help poorly dissolving drugs dissolve better, and sometimes as binders or stabilizers.
  • UNII ZH086O935Z
    A synthetic liquid used as a solvent and humectant (moisture-retaining agent) in medicines. It helps dissolve active ingredients and maintain the product's texture and stability.
  • 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 023XA5Z50L
    Hexamidine diisethionate is a synthetic antimicrobial compound used as a preservative in medicines. It prevents bacterial and fungal growth to maintain product safety and stability during storage.
  • UNII ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII 1I96OHX6EK
    A cyclic carbohydrate derived from plant starch that acts as a solubilizer and stabilizer. It helps dissolve poorly water-soluble drugs and protects active ingredients from degradation in the formulation.
  • 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 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • 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 5X73DDS97A
    A synthetic polymer used as a conditioning and antistatic agent. In medicines, it helps improve texture, reduce static buildup, and enhance how the product feels or flows.
  • UNII G2SH0XKK91
    Retinol is a form of vitamin A derived from animal sources or synthesized in a lab. In medicines, it may serve as an active therapeutic ingredient in some formulations, though when listed as an excipient it functions as a skin-conditioning agent or antioxidant to help stabilize the product.
  • 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.

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

The official label also statesAqua, Propanediol, Butylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Alcohol, Hydrogenated Castor Oil, Cyclodextrin,Diethoxydiglycol, Sodium Hydroxide,Retinol,Quaternium-73, Propylene Glycol,Phenoxyethanol, Ethylhexylglycerin,Hydroxypropyl Cyclodextrin, Hexamidine Diisethionate.

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

LabelerGuangzhou Senmai Biotechnology Co.,Ltd.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code84509
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio8 products on file

More NDCs from Guangzhou Senmai Biotechnology Co.,Ltd. labeler code 84509

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 📋 Description 📄 Do Not Use 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

Uses Clears Acne & Bumps,Fast Flattens Acne,Fades Acne Scars,Acne Treatment.After cleansing the skin,dip a cotton swab in thisproduct to apply the acne,and form a protective film when the product dries through.

⏱️ Dosage and Administration 6 words ▾

DOSAGE Approximately 0.01-0.02 oz each time.

⚠️ Warnings 7 words ▾

Warnings For external use only. Avoid contactwitheyes

🧪 Active Ingredient 26 words ▾

Active Ingredients ZINC OXIDE .......... 20% ............. Flattens Acne NIACINAMIDE....... 5% ...... Fades Acne Scars COLLOIDAL SULFUR ........3%.......Flattens Acne AZELAIC ACID.............2.4% .........Clears Acne SALICYLIC ACID...........1.8%............ anti-acne

🧪 Inactive Ingredients 24 words ▾

Inactive Ingredients Aqua, Propanediol, Butylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Alcohol, Hydrogenated Castor Oil, Cyclodextrin,Diethoxydiglycol, Sodium Hydroxide,Retinol,Quaternium-73, Propylene Glycol,Phenoxyethanol, Ethylhexylglycerin,Hydroxypropyl Cyclodextrin, Hexamidine Diisethionate.

🎯 Purpose 3 words ▾

Purpose Acne treatment

📋 Description 44 words ▾

Product Name PEGO Acne Buster Salicylic Acid Drying Serum

Manufacturer Guangzhou Senmai Biotechnology Co.,Ltd.

Address Floor 1-4,Building A,Guanger Smart Industrial Park,No.2 Qianyi East Road, Shiling Town,Huadu District,Guangzhou,Guangdong,CN(China)

Capacity 10ml / 0.34 fl.0z

Shelf Life Shelf Life ·3 Years

Place of Origin Made in PRC

📄 Do Not Use 8 words ▾

Do not use on damaged or broken skin.

📄 When Using This Product 63 words ▾

When using this product CAUTIONS 1. It is recommended to test the product behind the ear beforeuse. If discomfort is felt, do not use.2. If it accidentally enters the eyes, rinse immediately with water.3. Keep out of reach of children. Do not use for children under 3 years old.4. Do not expose to direct sunlight and high temperatures.5. This product contains salicylic acid.

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 1 words ▾

label

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 Senmai Biotechnology Co.,Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Senmai Biotechnology 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.
← 84509-0105-01 · Guangzhou 84509-0109-01 · Guangzhou →
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.