Label: WART REMOVER liquid
- NDC Code(s): 83299-010-01
- Packager: Consilii LLC
- 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 July 13, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
-
Directions
wash the affected area
may soak the wart in warm water for 5 minutes
dry area thoroughly
using the applicator(brush or cotton swab), apply one drop at a time to sufficiently cover each wart
allow it to fully absorb and let dry
repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks - Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WART REMOVER
wart remover liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83299-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 12 mg in 100 mL Inactive Ingredients Ingredient Name Strength CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS) STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) LONICERA CONFUSA WHOLE (UNII: 22L2C7GWOA) HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) ALBIZIA JULIBRISSIN BARK (UNII: 0J9G6W44DV) PODOPHYLLUM HEXANDRUM ROOT (UNII: 4YOL15R9R8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83299-010-01 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M028 07/12/2023 Labeler - Consilii LLC (118891890) Establishment Name Address ID/FEI Business Operations Consilii LLC 118891890 label(83299-010) , manufacture(83299-010)