Label: LIQUID WART REMOVER- salicylic acid liquid
- NDC Code(s): 79481-0614-1
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 1, 2024
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Flammable
- keep away from fire or flame
- cap bottle tightly and store at room temerature away from heat
Do not use
- if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
- on genital warts and warts on the face
- on moles, birthmarks and warts with hair growing from them
- on mucous membranes
- on irritated, infected or reddened skin
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Directions
- wash affected area, may soak wart in warm water for 5 minutes
- dry area thoroughly
- carefully apply small amount of wart remover with applicator to sufficiently cover each wart
- do not apply to face or neck
- let dry and repeat this procedure once or twice daily 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
LIQUID WART REMOVER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0614 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 170 mg in 1 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:79481-0614-1 1 in 1 CARTON 08/25/2023 1 9 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 08/25/2023 Labeler - Meijer Distribution Inc (006959555)