Label: PLANTAR WART REMOVERS- salicylic acid disc
- NDC Code(s): 73469-6331-2
- Packager: Scholls Wellness Company 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 May 26, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
- wash affected area and dry thoroughly
- if necessary, cut medicated disc to fit plantar wart
- apply medicated disc with sticky side adhering to skin
- covr medicated dosc with enclosed cushion
- after 48 hours, remove medicated disc
- repeat procedure every 48 hours as needed for up to 14 days (until plantar wart is removed)
- may soak plantar wart in warm water for 5 minutes to assist in removal
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PLANTAR WART REMOVERS
salicylic acid discProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73469-6331 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.4 g in 1 g Inactive Ingredients Ingredient Name Strength BROWN IRON OXIDE (UNII: 1N032N7MFO) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MINERAL OIL (UNII: T5L8T28FGP) ANTIOXIDANT GS (UNII: 2BBL73FIEU) TALC (UNII: 7SEV7J4R1U) WHITE PETROLATUM (UNII: B6E5W8RQJ4) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73469-6331-2 12 in 1 CARTON 05/31/2023 1 1 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M028 05/23/2023 Labeler - Scholls Wellness Company LLC (117174744) Registrant - Scapa Tapes North America LLC (079995435) Establishment Name Address ID/FEI Business Operations Scapa Tapes North America Inc. 079995435 manufacture(73469-6331)