SALICYLIC ACID- corn and callus remover liquid liquid

Salicylic Acid by

Drug Labeling and Warnings

Salicylic Acid by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. 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
• cap bottle tightly and store at room temperature away from heat

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, except under the advice and supervision of a doctor or podiatrist

When using this product

• avoid contact with eyes
• avoid inhaling vapors
• if product gets into the eye, flush with water for 15 minutes

Stop and ask a doctor if

discomfort persists, see your doctor or podiatrist.

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
• use cushion with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
• 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)

close tightly to prevent solidification

store in a cool place

Inactive ingredients

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-866-964-0939

Principal Display Panel

Rite Aid Pharmacy

LIQUID CORN & CALLUS REMOVER

Salicylic Acid 17

Safely removes corns & calluses ​ Soft foam cushions & protects

0.33 FL OZ (9.8 mL) 3 CUSHIONS

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
corn and callus remover liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.17 mg  in 9.8 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0120-9	9.8 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	12/22/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	12/22/2017

Labeler - Rite Aid Corporation (014578892)