SALICYLIC ACID- medicated callus removers patch

Salicylic Acid by

Drug Labeling and Warnings

Salicylic Acid by is a Otc medication manufactured, distributed, or labeled by HEB. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 40%

​Purpose

Callus remover

​Uses

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

​Warnings

​For external use only.

​Do not use

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

​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 right away.

​Directions

• wash affected area and dry thoroughly
• if necessary, cut medicated patch to fit callus
• apply adhesive side down of medicated patch onto callus
• cover medicated patch with pad
• after 48 hours, remove medicated patch
• repeat procedure every 48 hours as needed for up to 14 days (until callus is removed)
• may soak callus in warm water for 5 minutes to assist in removal

Other information

store between 15°C to 30°C (59°F to 86°F)

​Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

​Questions?

call 1-888-423-0139

Principal Display Panel

HILL COUNTRY ESSENTIALS
Medicated

Callus Removers
with Salicylic Acid

Callus Removal

Treatment

Protects Against Pressure & Pain

6 Pads/ 4 Medicated Patches

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
medicated callus removers patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-523
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  in 4

Inactive Ingredients
Ingredient Name	Strength
POLYVINYL ALCOHOL (UNII: 532B59J990)
VINYL ACETATE (UNII: L9MK238N77)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-523-04	4 in 1 PACKAGE; 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 - HEB (007924756)