Label: SALICYLIC ACID- callus removers patch
- NDC Code(s): 56104-013-04
- Packager: Premier Brands of America Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 11, 2024
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- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- wash affected area and dry thoroughly
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if necessary, cut medicated patch to fit callus
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apply adhesive side down of medicated patch onto callus
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cover medicated patch with pad
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after 48 hours, remove medicated patch
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repeat procedure every 48 hours as needed for up to 14 days (until callus is removed)
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may soak callus in warm water for 5 minutes to assist in removal
- continued wearing of pad (without patch) will help prevent recurrence of calluses
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
callus removers patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56104-013 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 4 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:56104-013-04 4 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M030 01/01/2013 Labeler - Premier Brands of America Inc. (063849780)