LIQUID CALLUS REMOVER- salicylic acid liquid

Liquid Callus Remover by

Drug Labeling and Warnings

Liquid Callus Remover by is a Otc medication manufactured, distributed, or labeled by Premier Brands of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 17% w/w

Purpose

Corn and callus remover

Uses

• for the removal of corns and calluses
• relieves pain by removing corns and calluses

Warnings

For external use only.

Flammable

• keep away from fire or flame

Do not use

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

When using this product

• if product gets into the eye, flush with water for 15 minutes
• avoid inhaling vapors
• cap bottle tightly and store at room temperature away from heat

Stop and ask a doctor if

discomfort persists

Keep out of reach of children.

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

Directions

• wash the affected area and dry thoroughly
• apply one drop at a time with applicator to sufficiently cover each corn/callus
• let dry
• repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
• may soak corn/callus in warm water for 5 minutes to assist in removal

Other information

• store between 20° to 25°C (68° to 77°F)
• avoid surrounding skin when applying product
• close tightly to prevent solidification
• wipe top of bottle clean after each use
• do not allow to come into contact with fabrics, floors, countertops or other surfaces -- will stain

Inactive ingredients

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

Principal Display Panel

EndZone

LIQUID

CALLUS

REMOVER

SALICYLIC ACID 17% / CORN & CALLUS REMOVER

Safely removes corns & calluses

0.33 FL OZ (9.8 mL)

INGREDIENTS AND APPEARANCE

LIQUID CALLUS REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-501
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	170 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CASTOR OIL (UNII: D5340Y2I9G)
PYROXYLIN (UNII: KYR8BR2X6O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-501-00	1 in 1 CARTON	09/11/2023
1		9.8 mL in 1 BOTTLE, WITH APPLICATOR; 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	09/11/2023

Labeler - Premier Brands of America Inc. (063849780)