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INVISIBLE ACNE PATCHES Salicylic Acid 0.5% .5 g/100g Patch, 96 patches — NDC 87843-0314-96 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

INVISIBLE ACNE PATCHES Salicylic Acid 0.5% .5 g/100g Patch, 96 patches — NDC 87843-314-96 (Billing 87843-0314-96)

by Global America Group LLC · 96 PATCH in 1 PACKAGE / .018 g in 1 PATCH

This is a package of 96 patches of INVISIBLE ACNE PATCHES Salicylic Acid 0.5% .5 g/100g Patch from Global America Group LLC, marketed since Aug 2026 and currently FDA-listed.

NDC 87843-0314-96
🏷️ FDA NDC (as labeled) 87843-314-96 billing pads the product segment with a zero
This package
Contains96 patches Pack sizes2 compare ↓
Product page 87843-0314-48 Also comes in: 48 patches 87843-314-48
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 17, 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) 87843-314-96
Product NDC 87843-314
11-digit billing NDC 87843031496
RxCUI 1994404
UNII O414PZ4LPZ
Application # M006
SPL Set ID 1527e15f-472f-4e05-adb6-c2e561f503cf
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-31
Route TOPICAL
Dosage form PATCH
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 1994404
Why two NDCs? The FDA registers this code as 87843-314-96 — 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 → 87843-0314-96. 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 is this product?

This is a topical patch containing salicylic acid 0.5% that is applied directly to the skin. Salicylic acid is commonly used in over-the-counter acne products to help exfoliate the outer layer of skin and unclog pores. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for this category of skin-care agent rather than undergoing individual product review.

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 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.
Try another pack size: 48 patches
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
87843-0314-48 87843-314-48 Main listing 48 PATCH in 1 PACKAGE / .018 g in 1 PATCH 2026-08-31 — Active
87843-0314-96 You're viewing this 96 PATCH in 1 PACKAGE / .018 g in 1 PATCH 2026-08-31 — Active

Pack size FAQ

What quantity is in this package?
This package contains 96 patches — 96 patch in 1 package / .018 g in 1 patch.
How does this package differ from NDC 87843-0314-48?
Both are INVISIBLE ACNE PATCHES Salicylic Acid 0.5% .5 g/100g Patch — the drug itself is identical. This page's package is the 96 patches one, while NDC 87843-0314-48 is the 48 patches package.
What NDC number is used to bill for this package of INVISIBLE ACNE PATCHES Salicylic Acid 0.5% .5 g/100g Patch?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Blemish Control Dots aloe vera .5 g/100g 56136-0185-01 Ganzhou 24 patches — — FDA listed —
Blemish Dots - Charcoal (10 Patches) .5 g/100g 56136-0188-01 Ganzhou 10 patches — — FDA listed —
My Beauty Spot Acne Buster .5 g/100g 56136-0183-01 Ganzhou 20 patches — — FDA listed —
my beauty spot BLEMISH DOTS - CHARCOAL (10 PATCHES) .5 g/100g 56136-0195-01 Ganzhou 10 patches — — FDA listed —
Blemish Dots - Charcoal (10 Patches) .5 g/100g 56136-0197-01 Ganzhou 10 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 56136-0199-01 Ganzhou 10 patches — — FDA listed —
Blemish Dots - Retinol (10 Patches) .5 g/100g 85588-0122-01 MELON 10 patches — — FDA listed —
My Beauty Spot Acne Buster .5 g/100g 56136-0182-01 Ganzhou 20 patches — — FDA listed —
Blemish Control Dots .5 g/100g 56136-0184-01 Ganzhou 24 patches — — FDA listed —
Blemish Dots - Retinol (10 Patches) .5 g/100g 56136-0187-01 Ganzhou 10 patches — — FDA listed —
Blemish Dots .5 g/100g 56136-0186-01 Ganzhou 10 patches — — FDA listed —
24 Pk Blemish Dot .5 g/100g 56136-0171-01 Ganzhou 24 patches — — FDA listed —
24 Pk Blemish Dot .5 g/100g 56136-0170-01 Ganzhou 24 patches — — FDA listed —
24 Pk Blemish Dot .5 g/100g 56136-0172-01 Ganzhou 24 patches — — FDA listed —
Invisible Acne Patches .5 g/100gthis 87843-0314-96 Global 96 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

🏛️
2026
On the market since
Aug 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.

What it looks like

ShapeRound
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 05JZI7B19X
    A plant-based thickener made from cellulose that holds water and creates texture. It works as a binder and thickening agent to give the medicine its proper consistency and help ingredients blend together.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.

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

The official label also statesHydrocolloid (CARBOXYMETHYLCELLULOSE), HYALURONIC ACID, TEA TREE OIL

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

LabelerGlobal America Group LLC
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code87843
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio6 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.
⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Package Label / Principal Display Panel
⏱️ Dosage and Administration 29 words ▾

DIRECTIONS 1. Clean and dry the area. 2. Peel patch from sheet. 3. Apply to blemish and press gently. Leave on for 6-8 hours or overnight. Figure1 Figure2 Figure3

⚠️ Warnings 48 words ▾

WARNINGS For external use only. Do not use on infected, cut, or irritated skin. Stop use and ask a doctor if rash or irrtation occurs. Keep out of reach of children Closed pores, blackheads, and unbroken red and swollen nodules are not suitable for treatmednt with this product.

🧪 Active Ingredient 5 words ▾

Active ingredient Salicylic Acid 0.5%

🧪 Inactive Ingredients 9 words ▾

INACTIVE INGREDIENTS Hydrocolloid (CARBOXYMETHYLCELLULOSE), HYALURONIC ACID, TEA TREE OIL

🎯 Purpose 3 words ▾

Purpose Acne treatment

📄 Package Label / Principal Display Panel 90 words ▾

PRINCIPAL DISPLAY PANEL GLOBAL AMERICA GROUP INVISIBLE ACNE PATCHES HYDROCOLLOID SPOT COVERS ULTRA-THIN • INVISIBLE • 0.5% Salicylic Acid 48 PATCHES 16 x 10mm • 16 x 12mm • 16 x 14mm WATER PROOF HYDROCOLLOID PROTECTS BLEMISHES VEGAN CRUELTY FREE CLEARER SKIN. MORE CONFIDENCE. Carton

PRINCIPAL DISPLAY PANEL GLOBAL AMERICA GROUP INVISIBLE ACNE PATCHES HYDROCOLLOID SPOT COVERS ULTRA-THIN • INVISIBLE • 0.5% Salicylic Acid 96 PATCHES 32 x 10mm • 32 x 12mm • 32 x 14mm WATER PROOF HYDROCOLLOID PROTECTS BLEMISHES VEGAN CRUELTY FREE CLEARER SKIN. MORE CONFIDENCE. Carton

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 Global America Group LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 48 patches (87843-0314-48). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Global America Group 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.
← 87843-0313-95 · Global 87843-0315-10 · Global →
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.