Label: SALICYLIC ACID- wart remover liquid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 24385-236-63 - Packager: AmerisourceBergen Drug Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 19, 2017
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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
- Directions
- Other information
- Inactive ingredients
- Questions?
- Principal Display Planel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
wart remover liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24385-236 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:24385-236-63 15 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/10/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358B 01/10/2012 Labeler - AmerisourceBergen Drug Corporation (007914906)