Label: SALICYLIC ACID- hydrogel clear wart remover patch
- NDC Code(s): 69842-294-09
- Packager: CVS Pharmacy
- 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 January 13, 2023
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- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- wash affected area, may soak wart in warm water for 5 minutes
- dry area thoroughly
- if necessary, cut medicated disc to fit wart
- apply adhesive side down of disc onto wart
- cover disc with cushions to conceal area
- repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
hydrogel clear wart remover patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-294 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 40 mg in 12 Inactive Ingredients Ingredient Name Strength HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) VINYL ACETATE (UNII: L9MK238N77) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-294-09 12 in 1 PACKAGE; Type 0: Not a Combination Product 02/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358F 02/01/2020 Labeler - CVS Pharmacy (062312574)