BIOPURE MEDICATED WART REMOVER STRIPS- salicylic acid, wart remover plaster

Biopure Medicated Wart Remover Strips by

Drug Labeling and Warnings

Biopure Medicated Wart Remover Strips by is a Otc medication manufactured, distributed, or labeled by QUEST USA CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic Acid 40%

Purpose

Wart Remover

Uses

• for the removal of common plantar warts. The common wart is easily recognized by the rough "cauliflower-like" appearance of the surface.

Warnings

For external use only.

Stop use and ask a doctor if

discomfort persists.

Do not use

on irritated skin or on any area that is infected or reddened skin

genital warts, or warts on the face

on moles, birthmarks, warts with hair growing from them

mucous membranes such as nose, anus, genitals and lips

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• wash affected area: may soak wart in warm water for 5 minutes
• dry area thoroughly
• peel off backing paper
• adhere medicated patch directly over wart
• repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

store between 59º and 86°F (15º and 30ºC)

Questions?

please call 1-718-975-2586

Inactive Ingridients

beeswax, oleo europaea (olive) fruit oil, paraffinum liquidum, glycerin, zinc oxide, pigment, silica

biopure. Medicated WART REMOVER STRIPS Maximum Strength salicylic acid removes warts safely and effectively 8 COUNT Single step method cushion Conceals & protects while removing warts

INGREDIENTS AND APPEARANCE

BIOPURE MEDICATED WART REMOVER STRIPS 
salicylic acid, wart remover plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-308
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
GLYCERIN (UNII: PDC6A3C0OX)
ZINC OXIDE (UNII: SOI2LOH54Z)
OLIVE OIL (UNII: 6UYK2W1W1E)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
MINERAL OIL (UNII: T5L8T28FGP)
YELLOW WAX (UNII: 2ZA36H0S2V)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78691-308-01	8 in 1 BOX	03/03/2025
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 Drug	M030	03/03/2025

Labeler - QUEST USA CORP (079869689)

Registrant - QUEST USA CORP (079869689)