A.H.C.COMPLETE CHOICE Moisture Ampoule

Drug Labeling and Warnings

Drug Details [pdf]

COMPLETE CHOICE MOISTURE AMPLOULE- adenosine liquid 
Carver Korea 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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A.H.C.
COMPLETE CHOICE Moisture Ampoule

Drug Facts

• Active Ingredients: Purpose
• Adenosine 0.04%: Skin Protectant

Uses

Help to improve skin moisture

Warning

For external use only

Do not use on damage or broken skin

Keep out of reach of Children.

Apply small amount to a clean skin and massage gently with fingertips.

Dosage: Small Amount

Administration: apply to a clean skin and massage gently

Inactive Ingredients

WATER
GLYCERIN
DIPROPYLENE GLYCOL
1,3-BUTYLENE GLYCOL
1,2-HEXANEDIOL
HYALURONATE SODIUM
TREHALOSE
PORTULACA OLERACEA WHOLE
PEG-40 CASTOR OIL
PEG/PPG-17/6 COPOLYMER
BENZYL ALCOHOL
PENTYLENE GLYCOL
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)
TROLAMINE
CARBOMER 1342
TREHALULOSE in 15 mL
HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT)
PANTHENOL
ALLANTOIN
VISCUM ALBUM WHOLE
IMPERATA CYLINDRICA ROOT
SOYBEAN GERM
PERILLA FRUTESCENS SEED
WITCH HAZEL
ALGINIC ACID
ORYZA SATIVA WHOLE
TARAXACUM OFFICINALE
CAMELLIA SINENSIS FLOWER
GARDEN SNAIL MUCIN
HYALURONIC ACID
ADANSONIA DIGITATA LEAF
OPUNTIA FICUS-INDICA
ALOE VERA LEAF
NELUMBO NUCIFERA GERM
DISODIUM HEDTA
LECITHIN, SOYBEAN
PHENOXYETHANOL

Bifida Ferment Lysate

Galactomyces Ferment Filtrate

Frangnance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPLETE CHOICE MOISTURE AMPLOULE 
adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58930-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	6 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TREHALOSE (UNII: B8WCK70T7I)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58930-017-02	1 in 1 CARTON	07/05/2013	12/01/2018
1	NDC: 58930-017-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/05/2013	12/01/2018

Labeler - Carver Korea Co.,Ltd (688442290)

Registrant - Jemian USA Inc. (078822273)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc.		689049693	manufacture(58930-017)

Revised: 6/2019

Document Id: a0dae587-8e49-4345-a710-f4df8b81f016

34390-5

Set id: d2797ae6-2c8c-475f-a2ed-3a7359d5d44c

Version: 2

Effective Time: 20190611