Label: SALICYLIC ACID- liquid wart remover liquid
- NDC Code(s): 70000-0329-1
- Packager: LEADER/ Cardinal Health 110, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 21, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Do not use
- if you are a diabetic or have poor blood circulation, except under the supervision of a doctor or podiatrist
- on irritated, infected or reddened skin
- on genital warts and warts on the face
- on moles, birthmarks and warts with hair growing from them
- on mucous membranes
- Directions
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
liquid wart remover liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0329 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 17 g in 100 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:70000-0329-1 1 in 1 CARTON 02/09/2018 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 02/09/2018 Labeler - LEADER/ Cardinal Health 110, Inc. (063997360)