DR. SCHOLLS ONE STEP CORN REMOVERS- salicylic acid disc

Dr. Scholls by

Drug Labeling and Warnings

Dr. Scholls by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic acid 40%

Purpose

Corn remover

Uses

• for removal of corns
• relieves pain by removing corns

Warnings

For external use only

Do not use

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

Stop use and ask a doctor if discomfort lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wash affected area and dry thoroughly
• apply medicated bandage
• after 48 hours , remove medicated bandage
• repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
• may soak corn in warm water for 5 minutes to assist in removal

Other information

▪ Store between 20° to 25°C (68° to 77°F).

▪ Protect from excessive heat (temperatures above 40°C (104°F)).

Inactive ingredients

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

Questions?

866-360-3226

PRINCIPAL DISPLAY PANEL - 6 Strip Carton

INGREDIENTS AND APPEARANCE

DR. SCHOLLS  ONE STEP CORN REMOVERS
salicylic acid disc

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-0753
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

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	brown (opaque solid)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-0753-1	6 in 1 CARTON	04/12/2005	04/30/2021
1		1 in 1 CELLO PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	04/12/2005	04/30/2021

Labeler - Bayer HealthCare LLC. (112117283)