CORN CARE PATCHES- salicylic acid patch

CORN CARE PATCHES by

Drug Labeling and Warnings

CORN CARE PATCHES by is a Otc medication manufactured, distributed, or labeled by Shenzhen Furuizhilian keji Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic acid 15%

PURPOSE

Corn and callus remover

INDICATIONS & USAGE

■ 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

■ if you have diabetes
■ if you have poor blood circulation
■ on irritated skin or any area that is infected or reddened

WHEN USING

■ if product gets in eyes, flush with water for 15 minutes
■ do not inhale vapors
■ store at room temperature away from heat

STOP USE

discomfort lasts

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

■ wash affected area and dry thoroughly
■ let dry
■ attach the patch to the affected area
■ repeat 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
■ protective pads may be used to cushion corn/callus during treatment
Children under 12 years of age:
consult a doctor

INACTIVE INGREDIENT

safflower, stemona, borneol, camphor

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CORN CARE PATCHES 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84445-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	9 g  in 60 g

Inactive Ingredients
Ingredient Name	Strength
STEMONA TUBEROSA ROOT (UNII: 7S9328671Z)
BORNEOL (UNII: M89NIB437X)
CAMPHOR, (-)- (UNII: 213N3S8275)
SAFFLOWER (UNII: 4VBL71TY4Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84445-008-01	60 g in 1 BOX; Type 0: Not a Combination Product	07/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	07/18/2024

Labeler - Shenzhen Furuizhilian keji Co., Ltd. (418598613)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Furuizhilian keji Co., Ltd.		418598613	manufacture(84445-008)