Capture C-Brightening Ampoule

Drug Labeling and Warnings

Drug Details [pdf]

CAPTURE C-BRIGHTENING AMPOULE- niacinamide 2% 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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Capture C-Brightening Ampoule

ACTIVE INGREDIENT

ACTIVE INGREDIENT

• Active Ingredients: Purpose
• Niacinamide 2%: Skin Protectant

Uses

Help to improve skin brightness

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
BIFIDOBACTERIUM LONGUM
GARDEN SNAIL MUCIN
DIPROPYLENE GLYCOL
1,2-HEXANEDIOL
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
PERILLA FRUTESCENS SEED
PORTULACA OLERACEA WHOLE
PEG-40 CASTOR OIL
MORUS ALBA BARK
LARICIFOMES OFFICINALIS WHOLE
ORYZA SATIVA WHOLE
TARAXACUM OFFICINALE ROOT
CAMELLIA SINENSIS WHOLE
ALLANTOIN
CAFFEINE
GLYCYRRHIZINATE DIPOTASSIUM
PUNICA GRANATUM WHOLE
FICUS CARICA WHOLE
CODONOPSIS LANCEOLATA ROOT
SOPHORA FLAVESCENS ROOT
CITRUS PARADISI WHOLE
MELIA AZEDERACH WHOLE
PRUNUS MUME FRUIT
EDETIC ACID
CITRUS AURANTIUM FRUIT OIL
CAMELLIA SINENSIS WHOLE
ORYZA SATIVA WHOLE
.ALPHA.-TOCOPHEROL ACETATE
3-O-ETHYL ASCORBIC ACID
ZANTHOXYLUM PIPERITUM FRUIT PULP
PULSATILLA KOREANA WHOLE
USNEA BARBATA
LECITHIN, SOYBEAN
XANTHAN GUM
HYALURONATE SODIUM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CAPTURE C-BRIGHTENING AMPOULE 
niacinamide 2% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58930-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)
CAFFEINE (UNII: 3G6A5W338E)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58930-036-01	1 in 1 CARTON	07/05/2013	12/01/2018
1		50 mL in 1 BOTTLE, DROPPER; 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
EYESOME. Co.,Ltd.		557795360	manufacture(58930-036)

Revised: 6/2019

Document Id: a378d604-4ca8-4256-a657-631fd1df21c2

34390-5

Set id: 5bc69455-d26f-4c53-af57-12a36d18b721

Version: 2

Effective Time: 20190607