Acne Drying

SALICYLIC ACID TOPICAL HUMAN OTC DRUG

Acne Drying is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by Spa de Soleil administered by TOPICAL. 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 20260430.

Generic name
SALICYLIC ACID
Manufacturer
Spa de Soleil
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
68062-9003
Application
M006
Label effective
20260430

About this product

Acne Drying is an FDA-registered drug product whose active ingredient is SALICYLIC ACID. It is labelled by Spa de Soleil taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 68062-9003, application M006, label effective 20260430. It is one of 265 FDA drug label records sharing the active ingredient SALICYLIC ACID. 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 are most often described in connection with: management acne. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Purpose Salicylic Acid (0.5%)..........Acne Medication

Indications & Usage

Use for the management of acne

Dosage & Administration

Directions: Cleanse skin thoroughly before applying medication . Cover the entire affected area with a thin layer one to two times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor . If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Warnings

Warnings: For external use only. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Sensitivity test for new users: Apply product sparingly to one or two small affected areas during the first three days. If no discomfort occurs, follow the steps stated in directions.

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How products containing SALICYLIC ACID compare

FDA lists 265 drug label records with SALICYLIC ACID 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 formProductsManufacturerProducts
— — L'Oreal USA Products Inc 20
— — Guangzhou Hechuang Commercial Service Co.,Ltd. 8
— — Kenvue Brands LLC 6
— — COSMETIQUE ACTIVE PRODUCTION 5
— — CVS Health 5

Frequently asked questions

What is Acne Drying used for?
Use for the management of acne

Who makes Acne Drying?
Spa de Soleil is the labeler of record for Acne Drying. 265 FDA label records share the active ingredient SALICYLIC ACID, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Acne Drying come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Acne Drying 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?
Yes. 265 FDA drug label records list SALICYLIC ACID 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 Drying 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.