Label: WART REMOVER LIQUID- salicylic acid liquid
- NDC Code(s): 21130-334-01
- Packager: Better Living Brands
- Category: HUMAN OTC DRUG LABEL
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 June 7, 2023
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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 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
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on irritated, infected or reddened skin
- Directions
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
WART REMOVER LIQUID
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-334 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:21130-334-01 1 in 1 CARTON 06/07/2023 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 final part358B 06/07/2023 Labeler - Better Living Brands (009137209)