Label: SALICYLIC ACID- wart remover liquid liquid
- NDC Code(s): 59779-500-09, 59779-500-15
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
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For external use only.
Do not use
- if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
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irritated, infected or reddened skin
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genital warts and warts on the face
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moles, birthmarks and warts with hair growing from them
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mucous membranes
- Directions
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SALICYLIC ACID
wart remover liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.17 mg in 15 mL Inactive Ingredients Ingredient Name Strength PYROXYLIN (UNII: KYR8BR2X6O) CAMPHOR (NATURAL) (UNII: N20HL7Q941) CASTOR OIL (UNII: D5340Y2I9G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-500-15 15 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/01/2014 2 NDC:59779-500-09 9 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 05/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 01/01/2014 Labeler - CVS Pharmacy (062312574)