Label: SALICYLIC ACID- medicated plantar wart remover patch
- NDC Code(s): 36800-378-24
- Packager: Topco Associates LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Active ingredient
- Purpose
- Uses
- 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 patch to fit wart
- apply the adhesive side of patch onto wart
- cover medicated patch with pad to conceal area
- repeat 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
medicated plantar wart remover patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-378 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 24 Inactive Ingredients Ingredient Name Strength POLYVINYL ALCOHOL (UNII: 532B59J990) VINYL ACETATE (UNII: L9MK238N77) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36800-378-24 24 in 1 BOX; Type 0: Not a Combination Product 12/06/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 12/06/2017 Labeler - Topco Associates LLC (006935977)