SALICYLIC ACID- one step corn remover 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%w/w

Purpose

   Corn Remover

Use

• For the removal of corns

Warnings

For external use only.

Do not use

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

Keep out of reach of children

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

If discomfort persists

see your doctor or podiatrist.

Directions

• wash affected area, may soak corn in warm water for 5 minutes
• dry area thoroughly
• remove bandage strips by peeling backing off at slit
• adhere medicated bandage directly over corn
• after 48 hours remove medicated bandage strip
• repeat this procedure every 48 hours as needed (until corn is removed) for up to 14 days.

Other Information

store between 59o and 86 oF (15 o and 30 oC)

Inactive ingredients

acrylic adhesive, brown iron oxide, polyethylene foam

Questions?

Call 1-866-964-0939

Principal Display Panel

HILL COUNTRY ESSENTIALS

Maximum Strength

One-Step Clear

Medicated

Corn Removers

with Salicylic Acid

Removes Corn

and Relieves Pain

6 MEDICATED CLEAR BANDAGES

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
one step corn remover patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-513
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 6

Inactive Ingredients
Ingredient Name	Strength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
BROWN IRON OXIDE (UNII: 1N032N7MFO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-513-06	6 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)