Label: MEDICATED PLANTAR WART REMOVER- salicylic acid patch
- NDC Code(s): 63940-162-01
- Packager: Harmon Store Inc.
- 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 18, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
-
Directions
- wash affected area, may soak wart in warm water for 5 minutes
- dry area thoroughly
- if necessary, cut medicated patch to fit wart
- carefully adhere medicated patch directly over 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?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
MEDICATED PLANTAR WART REMOVER
salicylic acid patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63940-162 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:63940-162-01 24 in 1 BOX; Type 0: Not a Combination Product 08/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358B 08/19/2022 Labeler - Harmon Store Inc. (804085293)