ISLEAF CUSHION CONCEALER 21- titanium dioxide liquid

isLeaf Cushion Concealer 21 by

Drug Labeling and Warnings

isLeaf Cushion Concealer 21 by is a Otc medication manufactured, distributed, or labeled by C3 Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

titanium dioxide

INACTIVE INGREDIENT

wter butylene glycol, beeswas, etc.

PURPOSE

brighten around eyes or face

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Click end to release product into brush, then apply to areas you want to perfect and brighten around eyes or face. Repeat until desired coverage is achieved, then pat into skin with fingertips to blend flawlessly.

WARNINGS

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight
2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight

4. Use as avoiding eye areas.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ISLEAF CUSHION CONCEALER 21 
titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70818-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1.6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70818-001-01	3.5 g in 1 APPLICATOR; Type 0: Not a Combination Product	08/08/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	08/08/2017

Labeler - C3 Co., Ltd. (689846633)

Registrant - C3 Co., Ltd. (689846633)

Establishment
Name	Address	ID/FEI	Business Operations
C3 Co., Ltd.		689846633	manufacture(70818-001) , label(70818-001) , pack(70818-001)