ISLEAF LONG LASTING WATERPROOF EYELINER BLACK- methylparaben liquid

isLeaf Long Lasting Waterproof Eyeliner Black by

Drug Labeling and Warnings

isLeaf Long Lasting Waterproof Eyeliner Black by is a Otc medication manufactured, distributed, or labeled by C3 Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

methylparaben

INACTIVE INGREDIENT

water, butylene glycol, alcohol, etc

PURPOSE

For a thin & delicate line

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

For a thin & delicate line, drag lightly the brush tip across the base of your lash line, pressing the brush as close to the lash roots as possible. To create a thinner line, use less pressure and add more pressure to create high-impact and a bolder line or continue to layer until you get desired eye look.

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 LONG LASTING WATERPROOF EYELINER BLACK 
methylparaben liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70818-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYLPARABEN (UNII: A2I8C7HI9T) (METHYLPARABEN - UNII:A2I8C7HI9T)	METHYLPARABEN	0.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70818-003-01	0.55 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
unapproved drug other		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(70818-003) , label(70818-003) , pack(70818-003)