NDC | 49035-019-04 |
Set ID | 83f3b428-e914-419b-8fa3-5444647a7061 |
Category | HUMAN OTC DRUG LABEL |
Packager | Wal-Mart Stores, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART358F |
- Active ingredient
- Purpose
- Uses
- Warnings
-
Directions
- wash affected area and dry thoroughly
- if necessary, cut medicated patches to fit callus
- apply the adhesive side down of medicated patch onto callus
- cover medicated patch with pad
- after 48 hours, remove medicated patch
- repeat procedure every 48 hours as needed for up to 14 days (until callus is removed)
- may soak callus in warm water for 5 minutes to assist in removal
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
EXTRA THICK CALLUS REMOVERS
extra thick callus removers with salicylic acid patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-019 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 100 mg 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:49035-019-04 160 mg in 1 PACKAGE; Type 0: Not a Combination Product 08/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358F 08/01/2013 Labeler - Wal-Mart Stores, Inc. (051957769)