Label: SALICYLIC ACID- wart remover gel gel
- NDC Code(s): 68016-632-00
- Packager: Chain Drug Consortium, LLC
- 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
- on moles, birth marks and warts with hair growing from them
- on mucous membranes such as nose, anus, genitals and lips
- on irritated, infected or reddened skin
- on genital warts and warts on the face
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Directions
- after washing affected area, soak wart in for 5 minutes in comfortably warm water
- dry area thoroughly
- gently squeeze a drop of gel from tube and apply to wart. Apply one drop at a time to sufficiently cover each wart
- let dry
- repeat this procedure once or twice daily (until wart is removed) for up to 12 weeks
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
wart remover gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-632 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 g in 7 g Inactive Ingredients Ingredient Name Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) ALCOHOL (UNII: 3K9958V90M) ETHYL ACETATE (UNII: 76845O8NMZ) HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PYROXYLIN (UNII: KYR8BR2X6O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68016-632-00 7 g in 1 TUBE; Type 0: Not a Combination Product 10/20/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 10/20/2011 Labeler - Chain Drug Consortium, LLC (101668460)