Label: SALICYLIC ACID- wart remover plaster
- NDC Code(s): 11822-0134-1
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Do not use this product if
you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
Do not use on
- irritated, infected or reddened skin
- moles, birthmarks and warts with hair growing from them on
- genital warts and warts on the face
- mucous membranes
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Directions
- after washing affected area, soak wart for 5 minutes in comfortably warm water
- dry area thoroughly
- if necessary cut medicated patch to fit wart
- apply adhesive side down of patch onto wart
- cover patch with pad to conceal area
- repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
wart remover plasterProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0134 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.4 g in 18 Inactive Ingredients Ingredient Name Strength HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0134-1 18 in 1 BOX; Type 0: Not a Combination Product 12/22/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 12/22/2017 Labeler - Rite Aid Corporation (014578892)