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Vanishing Skincare Vanishing Dry Serum Mask, Phase 3 .5 mg/100mg Patch, 1 mg — NDC 85059-0001-03 package photo

Vanishing Skincare Vanishing Dry Serum Mask, Phase 3 .5 mg/100mg Patch, 1 mg

by Vanish Skincare LLC · 1 mg in 1 PACKET (85059-001-03)
NDC 85059-0001-03
🏷️ FDA NDC (as labeled) 85059-001-03 billing pads the product 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) 85059-001-03
Product NDC 85059-001
11-digit billing NDC 85059000103
RxCUI 1994404
UNII O414PZ4LPZ
Application # M006
SPL Set ID 27f19c03-1a18-6c74-e063-6394a90a6e86
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-01-15
Route TOPICAL
Dosage form PATCH
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 85059-001-03 — 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 → 85059-0001-03. 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

LabelerVanish Skincare LLC
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code85059
First marketedJan 2025
Product typeHuman Otc Drug
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.

💊 What it looks like

Color white
ShapePENTAGON (5 sided)
Imprint1
Size3 mm
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesWater, Glycerin, Aloe Vera Leaf Juice, Lactic Acid, Glycolic Acid, Kaolin, Citric Acid, Fragrance.

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 eachPer 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
Lacura Blemish Dots Conceal and Treat 5 mg/g 56136-0181-01 Ganzhou 36 patches — — FDA listed —
My Beauty Spot Acne Buster .5 g/100g 56136-0182-01 Ganzhou 20 patches — — FDA listed —
My Beauty Spot Acne Buster .5 g/100g 56136-0183-01 Ganzhou 20 patches — — FDA listed —
Blemish Control Dots .5 g/100g 56136-0184-01 Ganzhou 24 patches — — FDA listed —
Blemish Control Dots aloe vera .5 g/100g 56136-0185-01 Ganzhou 24 patches — — FDA listed —
Blemish Dots .5 g/100g 56136-0186-01 Ganzhou 10 patches — — FDA listed —
Blemish Dots - Retinol (10 Patches) .5 g/100g 56136-0187-01 Ganzhou 10 patches — — FDA listed —
Blemish Dots - Charcoal (10 Patches) .5 g/100g 56136-0188-01 Ganzhou 10 patches — — FDA listed —
Healing Blemish Dots .5 g/100g 56136-0189-01 Ganzhou 16 patches — — FDA listed —
MY BEAUTY SPOT Acne Care Patch Kit .5 g/100g 56136-0190-01 Ganzhou 40 patches — — FDA listed —
Healing Acne Care Patches - Tea Tree and Vitamin A .5 g/100g 56136-0191-01 Ganzhou 150 patches — — FDA listed —
Healing Acne Care Patches - Tea Tree and Salicylic Acid .5 g/100g 56136-0192-01 Ganzhou 150 patches — — FDA listed —
my beauty spot BLEMISH DOTS - CHARCOAL (10 PATCHES) .5 g/100g 56136-0195-01 Ganzhou 10 patches — — FDA listed —
acne buster star patch 140 patches - Tea Tree Extract and Salicylic Acid .5 g/100g 56136-0196-01 Ganzhou 140 patches — — FDA listed —
Blemish Dots - Charcoal (10 Patches) .5 g/100g 56136-0197-01 Ganzhou 10 patches — — FDA listed —
ACNE DOTS (Skin Care Multi-Pack) .5 g/100g 56136-0198-01 Ganzhou 24 patches — — FDA listed —
Blemish Dots - Retinol (10 Patches) .5 g/100g 56136-0199-01 Ganzhou 10 patches — — FDA listed —
Peace Out Acne .359 mg 71494-0001-20 Peace 20 patches — — FDA listed —
Peace Out Acne Day and Night Duo 71494-0003-20 Peace 10 patches — — FDA listed —
Peace Out Acne Day and Night Duo 71494-0004-40 Peace 20 patches — — FDA listed —
Peace Out Acne .359 mg 71494-0006-20 Peace 20 patches — — FDA listed —
Peace Out Acne .5 mg 71494-0101-20 Peace 20 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78882-0401-35 Hangzhou 140 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78882-0402-10 Hangzhou 40 patches — — FDA listed —
Acne Dots 5 mg/1000mg 78936-0401-10 Hangzhou 40 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78936-0405-10 Hangzhou 40 patches — — FDA listed —
Acne Healing Dots 5 mg/1000mg 78936-0407-09 Hangzhou 36 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78936-0409-38 Hangzhou 150 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78936-0411-10 Hangzhou 40 patches — — FDA listed —
Acne Dots 5 mg/1000mg 78936-0415-09 Hangzhou 36 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78936-0417-35 Hangzhou 140 patches — — FDA listed —
Acne Buster 5 mg/1000mg 78936-0419-10 Hangzhou 40 patches — — FDA listed —
Dissolvable Microneedle Blemish Patches 5 mg/1000mg 84895-0101-06 Advaccine 6 patches — — FDA listed —
Dissolvable Microneedle Blemish Patches 5 mg/1000mg 84895-0102-06 Advaccine 6 patches — — FDA listed —
Vanishing Skincare .5 mg/100mgthis 85059-0001-03 Vanish 1 mg — — FDA listed —
MY BEAUTY SPOT Day and Night Acne Patch .5 g/100g 85588-0101-01 MELON 40 patches — — FDA listed —
Blemish Dots - Charcoal (10 Patches) .5 g/100g 85588-0121-01 MELON 10 patches — — FDA listed —
Blemish Dots - Retinol (10 Patches) .5 g/100g 85588-0122-01 MELON 10 patches — — 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

🏛️
2025
On the market since
Jan 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85059-0001-03 You're viewing this 1 mg in 1 PACKET (85059-001-03) 2025-01-15 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 85059-001-03, 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: 85059-0001-03, written without dashes as 85059000103. 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 85059-0001-03, the first segment (85059) is the labeler code FDA assigned to Vanish Skincare LLC; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 Vanish Skincare LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Vanish Skincare 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.

📄 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 💊 Dosage Forms and Strengths ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 15 words ▾

Helps exfoliate and renew skin for a smoother, brighter appearance. Hydrates and improves skin texture.

⏱️ Dosage and Administration 32 words ▾

1. Cleanse face thoroughly. 2. Apply the mask to dry skin, avoiding contact with eyes. 3. Leave on for 15-20 minutes andremove gently. 4. Use once or twice a week as needed.

💊 Dosage Forms and Strengths 32 words ▾

Dosage Apply a thin, even layer to clean, dry skin. Leave on for 10–15 minutes. Rinse thoroughly with warm water. Use 1–2 times per week or as directed by a healthcare provider."

⚠️ Warnings 47 words ▾

Warning Section For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if rash or irritation occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active Ingredient(s) Active Ingredient: Salicylic Acid 0.5%.

🧪 Inactive Ingredients 14 words ▾

Water, Glycerin, Aloe Vera Leaf Juice, Lactic Acid, Glycolic Acid, Kaolin, Citric Acid, Fragrance.

🎯 Purpose 4 words ▾

Exfoliation and skin renewal.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85057-0001-01 · Simply 85060-0001-01 · Shantou →
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.