Bliss Care Acne Treatment Gel Salicylic Acid 2 g/100mL Gel, 10 mL
by Guangdong Aimu Biological Technology Co., Ltd · 10 mL in 1 TUBE (83566-627-01)
NDC 83566-0627-01
🏷️ FDA NDC (as labeled)
83566-627-01
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Sep 25, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
83566-627-01
Product NDC
83566-627
11-digit billing NDC
83566062701
Application #
M006
SPL Set ID
5bb8bc5b-e9ae-eb59-e063-6394a90a8029
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-09-18
Route
TOPICAL
Dosage form
GEL
Substance
SALICYLIC ACID
Why two NDCs?
The FDA registers this code as 83566-627-01 — 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 → 83566-0627-01. 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.
🏭 Manufacturer & labeler
LabelerGuangdong Aimu Biological Technology Co., Ltd
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code83566
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio39 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 is this product?
This is a topical gel containing salicylic acid, an over-the-counter skin-care product marketed under FDA's monograph rules for acne treatments. Salicylic acid is commonly used in acne products to help exfoliate skin and reduce oiliness. The gel form is applied directly to the skin surface. This product is not individually reviewed by the FDA but follows established safety and ingredient standards for nonprescription acne medications.
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.
💬 Questions about Salicylic Acid?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 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.
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UNII 19NOL5474Q
Isopentyldiol is a synthetic alcohol derived from isoprene. It functions as a humectant and solvent in formulations, helping to retain moisture and dissolve or suspend active ingredients.
-
UNII 4LVZ0Z0ITT
A plant seed ingredient used as a natural flavoring agent and filler. It adds taste and helps give the medicine its structure and volume.
-
UNII 05I15JNI2J
A synthetic polymer that absorbs and holds moisture. Used in tablets and capsules as a super-disintegrant to help the medicine break apart quickly when swallowed, allowing faster drug release.
-
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.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also stateswater,butylene glycol,nigella sativa seed extract,isopentyldiol,sodium polyacrylate
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 system | Per g | 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Cleansing Wipes 2 g/100mL 71613-0001-01 | Nextcell | 25 applicators | — | — | FDA listed | — |
| Oxygenetix Oxygenating Foundation Acne Control 2 g/100mL 10258-0101-11 | COLONIAL | 15 ml | — | — | Discontinued | — |
| Spot Stopper Acne Spot Treatment 2 g/100mL 69366-0412-32 | The | 1 tube | — | — | FDA listed | — |
| Pert 2 in 1 Advanced plus 2 g/100mL 81277-0802-13 | Sodalis | 400 ml | — | — | FDA listed | — |
| Eradikate Acne Mark Fading 2 g/100mL 43479-0112-51 | KATE | 1 bottle | — | — | FDA listed | — |
| Acne Control Face Wash 2 g/100mL 54111-0185-01 | Bentley | 180 ml | — | — | FDA listed | — |
| Salicylic Wash 2 g/100mL 70764-0102-56 | CONTROL | 1 bottle | — | — | FDA listed | — |
| Acne Spot Treatment 2 g/100mL 70764-0105-51 | CONTROL | 1 bottle | — | — | FDA listed | — |
| Acne Correction Pads 2 g/100mL 72957-0012-01 | Private | 1 jar | — | — | FDA listed | — |
| Multi-Action Clear - Acne Clearing Treatment 2% Salicylic Acid 2 g/100mL 76147-0301-07 | StriVectin | 1 tube | — | — | FDA listed | — |
| PanOxyl Acne Gel Wash 2 g/100mL 00316-0299-01 | Crown | 192 ml | — | — | FDA listed | — |
| PCA Gel 2 g/100mL 68726-0445-02 | CP | 1 bottle | — | — | FDA listed | — |
| First Aid Beauty FAB Acne Spot Treatment 2 g/100mL 69423-0724-22 | The | 1 tube | — | — | FDA listed | — |
| SEYTU Spot 2 g/100mL 84271-0002-00 | Omnilife | 1 tube | — | — | FDA listed | — |
| Pharma Clear Cleanser 2 g/100mL 67879-0101-11 | PHARMAGEL | 175 ml | — | — | FDA listed | — |
| Start So Fresh 2 g/100mL 70626-0105-13 | ASPIRE | 100 ml | — | — | FDA listed | — |
| Treat So Deep Acne-Fighting Treatment 2 g/100mL 70626-0106-15 | ASPIRE | 1 tube | — | — | FDA listed | — |
| Good Molecules Acne Foaming Cleanser 2 g/100mL 82730-0100-05 | Good | 148 ml | — | — | FDA listed | — |
| Acne Toner Serum 2 g/100mL 82870-0003-01 | Dime | 60 ml | — | — | FDA listed | — |
| Acne Spot Treatment 2 g/100mL 82870-0006-01 | Dime | 15 ml | — | — | FDA listed | — |
| Acne Control Superclean Body Wash AHA BHA Formula 2 g/100mL 54111-0170-50 | Bentley | 250 ml | — | — | FDA listed | — |
| Tula Skincare Clear It Up Acne Clearing and Tone Correcting Gel 2 g/100mL 84126-0121-15 | The | 1 tube | — | — | FDA listed | — |
| Tula Skincare Breakout Star Lightweight Acne Moisturizer 2 g/100mL 84126-0229-15 | The | 15 ml | — | — | FDA listed | — |
| Perricone MD Acne Relief Maximum Strength Clearing Treatment 2 g/100mL 84448-0301-59 | THG | 1 bottle | — | — | FDA listed | — |
| Perricone MD Acne Relief Gentle and Soothing Cleanser 2 g/100mL 84448-0539-17 | THG | 1 tube | — | — | FDA listed | — |
| Clearasil Stubborn Acne Control 5in1 Exfoliating Wash 2 g/100mL 63824-0436-01 | Reckitt | 200 ml | — | — | FDA listed | — |
| ELF Blemish Control Face Primer Clear 2 g/100mL 76354-0210-10 | e.l.f. | 30 ml | — | — | FDA listed | — |
| Curology Acne-Clearing Gel Serum 2 g/100mL 82575-0500-00 | Curology, | 1 tube | — | — | FDA listed | — |
| First Aid Beauty Acne Clearing Pads 2 g/100mL 84126-0119-60 | The | 60 patches | — | — | FDA listed | — |
| Perricone MD Acne Relief Calming and Soothing Clay Mask 2 g/100mL 84448-0955-10 | THG | 10 ml | — | — | FDA listed | — |
| Proactiv Deep Cleansing Wash 2 g/100mL 11410-0048-05 | THE | 1 bottle | — | — | FDA listed | — |
| Good Molecules Acne Foaming Cleanser 2 g/100mL 64412-1005-02 | Twincraft | 1 bottle | — | — | FDA listed | — |
| ELF Clear Blemish Control Face Primer 2 g/100mL 76354-0624-01 | e.l.f. | 14 ml | — | — | FDA listed | — |
| Ultra Clear Treatment 2 g/100mL 10028-0051-01 | ULTRACEUTICALS | 50 ml | — | — | FDA listed | — |
| Clear System Clarifying Gel Cleanser 2 g/100mL 54111-0189-20 | Bentley | 20 ml | — | — | FDA listed | — |
| anna lotan PURIFYING PADS with 2% Salicylic Acid 2 g/100mL 76446-0039-50 | Anna | 1 jar | — | — | Discontinued | — |
| Clarifying Peel 2 g/100mL 46007-0102-11 | Skin | 20 ml | — | — | Discontinued | — |
| Acne Control Body Wash 2 g/100mL 54111-0184-01 | Bentley | 250 ml | — | — | FDA listed | — |
| Clear Exfoliating Solution Paulas Choice 2 g/100mL 56152-5002-01 | Cosmetic | 118 ml | — | — | FDA listed | — |
| Bha Cleanser 2% 2 g/100mL 61328-0403-01 | Skinfix, | 30 ml | — | — | FDA listed | — |
| Eradikate Acne Mark Fading 2 g/100mL 72204-0903-02 | Rare | 1 bottle | — | — | FDA listed | — |
| Triderma Psoriasis Control Body Wash 2 g/100mL 10738-0217-63 | Genuine | 473 ml | — | — | FDA listed | — |
| Proactivplus Pore Clearing Treatment 2 g/100mL 11410-0047-30 | Alchemee, | 1 tube | — | — | FDA listed | — |
| First Aid Beauty FAB Pharma White Clay Acne Treatment 2 g/100mL 69423-0555-60 | The | 60 patches | — | — | FDA listed | — |
| ESSENCE BY CATHERINE HINDS PURIFYING PADS with 2% Salicylic Acid 2 g/100mL 76446-0022-50 | Anna | 1 jar | — | — | FDA listed | — |
| Good Molecules Maximum Strength Acne Gel Cream 2 g/100mL 82730-0102-01 | Good | 1 tube | — | — | FDA listed | — |
| Dry It Out Acne Spot Treatment 2 g/100mL 61197-0122-00 | Pacifica | 29 ml | — | — | FDA listed | — |
| Acne Spot Treatment 2% Bha 2 g/100mL 61328-0404-05 | Skinfix, | 15 ml | — | — | FDA listed | — |
| Clearasil Rapid Rescue Deep Treatment Wash 2 g/100mL 63824-0432-01 | Reckitt | 200 ml | — | — | FDA listed | — |
| Good Molecule Maximum Strenght Acne 2 g/100mL 68577-0287-00 | COSMAX | 1 tube | — | — | FDA listed | — |
| ORLASKIN ACNE Treatment 2 g/100mL 87582-0005-01 | Guangzhou | 50 ml | — | — | FDA listed | — |
| SUZANOBAGIMD Acne Cleansing Wipes 2 g/100mL 62032-0617-25 | Obagi | 25 patches | — | — | FDA listed | — |
| Bliss Care Acne Treatment Gel 2 g/100mLthis 83566-0627-01 | Guangdong | 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
Sep 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.
📊 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 83566-0627-01 You're viewing this | 10 mL in 1 TUBE (83566-627-01) | 2026-09-18 | 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 83566-627-01, 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: 83566-0627-01, written without dashes as 83566062701. 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 83566-0627-01, the first segment (83566) is the labeler code FDA assigned to Guangdong Aimu Biological Technology Co., Ltd; the middle segment (0627) 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 Guangdong Aimu Biological Technology Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangdong Aimu Biological Technology 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.
📄 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.
📄 FDA label ▾
No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.
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 ↗
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.