EQUATE ONE STEP WART REMOVER STRIPS- salicylic acid plaster

Equate One Step Wart Remover Strips by

Drug Labeling and Warnings

Equate One Step Wart Remover Strips by is a Otc medication manufactured, distributed, or labeled by Walmart Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic acid 40%

Purpose

Wart Remover

Uses

• for the removal of common and plantar warts
• the common wart is easily recognized by the rough “cauliflower-like” appearance of the surface
• the plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the footprint pattern

Warnings

For external use only.

Do not use

• on irritated skin or on any area that is infected or reddened
• on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes
• if you have diabetes or poor blood circulation

Stop use and ask a doctor if

discomfort persists.

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 59° and 86°F (15° and 30°C)

Inactive ingredients

lanolin, paraffin, petrolatum.

Questions or comments?

1-888-287-1915

Package Labeling:

INGREDIENTS AND APPEARANCE

EQUATE ONE STEP WART REMOVER STRIPS 
salicylic acid plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-226
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	40 mg

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-226-01	1 in 1 BOX	10/12/2023
1		14 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	M028	10/12/2023

Labeler - Walmart Inc. (051957769)