Acne Free SENSITIVE SKIN 24 HR Acne Clearing System
Acne Free SENSITIVE SKIN 24 HR Acne Clearing System is an FDA drug label for the active ingredient SALICYLIC ACID, BENZOYL PEROXIDE manufactured by AcneFree LLC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260731.
- Generic name
- SALICYLIC ACID, BENZOYL PEROXIDE
- Manufacturer
- AcneFree LLC
- Product type
- HUMAN OTC DRUG
- Route
- N/A
- Dosage form
- N/A
- NDC
- 80861-007
- Application
- M006
- Label effective
- 20260731
About this product
Acne Free SENSITIVE SKIN 24 HR Acne Clearing System is an FDA-registered drug product whose active ingredient is SALICYLIC ACID, BENZOYL PEROXIDE. It is labelled by AcneFree LLC and marketed as a human otc drug product. Identifiers on file: NDC 80861-007, application M006, label effective 20260731. It is one of 3 FDA drug label records sharing the active ingredient SALICYLIC ACID, BENZOYL PEROXIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing SALICYLIC ACID, BENZOYL PEROXIDE are most often described in connection with: treatment acne. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use for the treatment of acne
Dosage & Administration
Directions • use every morning and evening • apply a dime-size amount to damp skin and gently massage, avoiding the eye area • rinse well • if bothersome dryness or peeling occurs, reduce application use • may be used on chest or back
Warnings
Warnings For external use only When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
More products with the same ingredient
SALICYLIC ACID, BENZOYL PEROXIDESkin Pharmacy Advanced Acne Therapy Kit
View labelSkinPharmacy Advanced Acne Therapy Kit
View labelHow products containing SALICYLIC ACID, BENZOYL PEROXIDE compare
FDA lists 3 drug label records with SALICYLIC ACID, BENZOYL PEROXIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | AMCOL Health & Beauty Solutions, Inc. DBA | 1 |
| — | — | AcneFree LLC | 1 |
| — | — | CVS Health | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Acne Free SENSITIVE SKIN 24 HR Acne Clearing System used for?
Use for the treatment of acne
Who makes Acne Free SENSITIVE SKIN 24 HR Acne Clearing System?
AcneFree LLC is the labeler of record for Acne Free SENSITIVE SKIN 24 HR Acne Clearing System. 3 FDA label records share the active ingredient SALICYLIC ACID, BENZOYL PEROXIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
Is Acne Free SENSITIVE SKIN 24 HR Acne Clearing System prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing SALICYLIC ACID, BENZOYL PEROXIDE?
Yes. 3 FDA drug label records list SALICYLIC ACID, BENZOYL PEROXIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Acne Free SENSITIVE SKIN 24 HR Acne Clearing System been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.