CELLXV REAL KELP FACIAL MASK- arbutin, adenosine liquid

CELLXV REAL KELP FACIAL MASK by

Drug Labeling and Warnings

CELLXV REAL KELP FACIAL MASK by is a Otc medication manufactured, distributed, or labeled by WORLDCOSTEC.CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Arbutin, Adenosine

INACTIVE INGREDIENT

Water, Butylene Glycol, Etc

PURPOSE

Skin Protectant

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children

INDICATIONS & USAGE

Wash and dry your face thoroughly. Remove both sides of film and place upper and lower masks onto face. Leave on for 25~45min. Then remove masks and gently massage your face until the essence is fully absorbed.

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

CELLXV REAL KELP FACIAL MASK 
arbutin, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71450-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.03 g  in 100 mL
ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF)	ARBUTIN	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71450-0010-1	20 mL in 1 PACKAGE; Type 0: Not a Combination Product	05/26/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/26/2017

Labeler - WORLDCOSTEC.CO.,LTD (688297917)

Registrant - WORLDCOSTEC.CO.,LTD (688297917)

Establishment
Name	Address	ID/FEI	Business Operations
WORLDCOSTEC.CO.,LTD		688297917	manufacture(71450-0010) , label(71450-0010) , pack(71450-0010)