ABALONE CRYSTALDOUBLE EX AMPOULE- arbutin, adenosine liquid

ABALONE CRYSTALDOUBLE EX AMPOULE by

Drug Labeling and Warnings

ABALONE CRYSTALDOUBLE EX AMPOULE by is a Otc medication manufactured, distributed, or labeled by C&BCOSMETIC Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Arbutin, Adenosine

INACTIVE INGREDIENT

Water, Glycerin, Butylene Glycol, Etc.

PURPOSE

Skin Protectant - Anti-Wrinkle & Whitening

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

Take 1EA of ampoule on the palm entirely

Mixing well with fingertips and gently tapping along the skin texture for absorption

Even if you do not apply emulsion or cream, you can feel the moistness until next morning

*1EA of crystal Double-EX Ampoule is a throwaway product

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ABALONE CRYSTALDOUBLE EX AMPOULE 
arbutin, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60611-0006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF)	ARBUTIN	2.2 g  in 100 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.044 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60611-0006-1	14 in 1 PACKAGE	03/10/2017
1		0.8 mL in 1 SYRINGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/10/2017

Labeler - C&BCOSMETIC Co.,Ltd. (689909208)

Registrant - C&BCOSMETIC Co.,Ltd. (689909208)

Establishment
Name	Address	ID/FEI	Business Operations
C&BCOSMETIC Co.,Ltd.		689909208	manufacture(60611-0006) , label(60611-0006) , pack(60611-0006)