Label: SALICYLIC ACID- medicated plantar wart remover patch
- NDC Code(s): 59779-138-24
- 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 July 16, 2021
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- if you are diabetic or have poor blood circulation, except under the advise and supervision of a doctor or podiatrist
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on irritated, infected or reddened skin
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on genital warts and warts on the face
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on moles, birthmarks and warts with hair growing from them
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on mucous membranes
- Directions
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
medicated plantar wart remover patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-138 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:59779-138-24 24 in 1 BOX; Type 0: Not a Combination Product 01/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358B 01/01/2014 Labeler - CVS Pharmacy (062312574)