PLANTAR WART REMOVERS- salicylic acid disc

Plantar Wart Removers by

Drug Labeling and Warnings

Plantar Wart Removers by is a Otc medication manufactured, distributed, or labeled by Scholls Wellness Company LLC, Scapa Tapes North America LLC, Scapa Tapes North America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Salicylic acid 40%

PURPOSE

Purpose

Plantar Wart Remover

INDICATIONS & USAGE

• for the removal of plantar wart
• relieves pain by removing plantar wart

WARNINGS

For external use only

DO NOT USE

• if you are a diabetic
• if you have poor blood circulation
• on irritated skin or any aea that is infected or reddened

ASK DOCTOR

Stop use and ask a doctor if discomfort lasts

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

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

• store between 20° to 25°C (68° to 77°F)
• protect from excessive heat and temperatures above 40°C (140°F)

INACTIVE INGREDIENT

Inactive ingredients

Antioxidant (CAS 991-84-4), iron oxides, mineral oil, petroleum hydrocarbon resin, silicon dioxide, synthetic polyisoprene rubber, talc

QUESTIONS

Questions?

1-866-360-3226

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PLANTAR WART REMOVERS 
salicylic acid disc

Product 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 Drug	M028	05/23/2023

Labeler - Scholls Wellness Company LLC (117174744)