ABALONE CRYSTALDOUBLE EX AMPOULE- arbutin, adenosine liquid 
C&BCOSMETIC Co.,Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Arbutin, Adenosine

Water, Glycerin, Butylene Glycol, Etc.

Skin Protectant - Anti-Wrinkle & Whitening

keep out or reach of the children


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

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

for external use only

label

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)

Revised: 3/2017
Document Id: 4a58190e-39d8-38bb-e054-00144ff8d46c
Set id: 4a58190e-39d7-38bb-e054-00144ff8d46c
Version: 1
Effective Time: 20170310
 
C&BCOSMETIC Co.,Ltd.