Clearasil Rapid Rescue Deep Treatment Wash

SALICYLIC ACID TOPICAL HUMAN OTC DRUG

Clearasil Rapid Rescue Deep Treatment Wash is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by Reckitt Benckiser LLC 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 20260513.

Generic name
SALICYLIC ACID
Manufacturer
Reckitt Benckiser LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
63824-432
Application
M006
Label effective
20260513

About this product

Clearasil Rapid Rescue Deep Treatment Wash is an FDA-registered drug product whose active ingredient is SALICYLIC ACID. It is labelled by Reckitt Benckiser LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 63824-432, application M006, label effective 20260513. 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: treatment acne. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Salicylic acid 2%

Indications & Usage

Use for the treatment of acne

Dosage & Administration

Directions wet face dispense product into hands, lather and massage gently onto face and neck, avoiding the delicate eye area rinse thoroughly with warm water and pat dry 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 When using this product avoid contact with the eyes. If product gets into the eyes, rinse thoroughly with water. 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. limit use to the face and neck Stop use and ask a doctor if skin or eye irritation develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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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

Recall and safety notices

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-1517-2016 Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC 63824-207-60 Reckitt Benckiser LLC Class III Terminated 20160928
D-1363-2015 Mucinex Fast Max Cold, Flu & Sore Throat, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Dextromethorphan HBr Cough Suppressant, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Ages 12+, , Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-015-66, UPC 63824-01565-1 Reckitt Benckiser LLC Class I Terminated 20150902
D-1365-2015 Mucinex Fast-Max Cold & Sinus, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Ages 12+, Dist. by: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-016-66, UPC 63824-01665-8 Reckitt Benckiser LLC Class I Terminated 20150902
D-1367-2015 Mucinex Fast Max Severe Congestion & Cough, Maximum Strength, Dextromethorphan HBr Cough Suppressant, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC 63824-014-66, UPC 6382401465-4 Reckitt Benckiser LLC Class I Terminated 20150902
D-1368-2015 Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu, Maximum Strength, Two - 6 fl oz (180 mL) bottles Total - 12 fl oz (360 mL), For Ages 12+, Dist. by Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC 63824-528-22-01, NDC 63824-528-22-00, UPC 63824-52822-9 Reckitt Benckiser LLC Class I Terminated 20150902

Frequently asked questions

What is Clearasil Rapid Rescue Deep Treatment Wash used for?
Use for the treatment of acne

Who makes Clearasil Rapid Rescue Deep Treatment Wash?
Reckitt Benckiser LLC is the labeler of record for Clearasil Rapid Rescue Deep Treatment Wash. 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 Clearasil Rapid Rescue Deep Treatment Wash 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 Clearasil Rapid Rescue Deep Treatment Wash 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 Clearasil Rapid Rescue Deep Treatment Wash been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.