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%

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

PURPOSE

Corn and callus remover

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CORN CARE PATCHES 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84445-011
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1.5 g  in 30

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84445-011-01	30 in 1 BOX; Type 0: Not a Combination Product	08/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/08/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Furuizhilian keji Co., Ltd.		418598613	manufacture(84445-011)