Label: QUICK ACTION- salicylic acid swab
- NDC Code(s): 49035-666-18
- Packager: Equate
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 23, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- use
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three 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 directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Other information
- Inactive ingredients
- Questions?
-
adversa reacation
This product is not manufactured or distributed by Reckitt Benckiser, distributor of Clearasil ULTRA Rapid Action Pads
Satisfaction guaranteed-For Questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915
Distributed by: Wal-Mart Stores, Inc.,
Bentonville, AR 72716
- principal display panel
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INGREDIENTS AND APPEARANCE
QUICK ACTION
salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-666 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) ISOCETETH-20 (UNII: O020065R7Z) SORBITOL (UNII: 506T60A25R) SODIUM HYDROXIDE (UNII: 55X04QC32I) LAVANDULA STOECHAS WHOLE (UNII: MTZ2ZA34ZV) HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24) CISTUS MONSPELIENSIS LEAF (UNII: 1IE70KNO43) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-666-18 150 mL in 1 CONTAINER; Type 0: Not a Combination Product 06/21/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/21/2016 Labeler - Equate (051957769) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(49035-666) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(49035-666)