5 DAYS WHITENING BOOSTER liquid

5 DAYS WHITENING BOOSTER by

Drug Labeling and Warnings

5 DAYS WHITENING BOOSTER by is a Otc medication manufactured, distributed, or labeled by Guangzhou Kadiya Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Uses：
For facial whitening

INACTIVE INGREDIENT

AQUA、PROPYLENE GLYCOL、GLYCERETH-26、PENTAERYTHRITYL、TETRAETHYLHEXANOATE、ETHYLHEXYL PALMITATE、GLYCERIN、CETEARYL ALCOHOL、HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE、COPOLYMER、DMDM HYDANTOIN、XANTHAN GUM、CETEARYL GLUCOSIDE、AROMA、GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER、CI 19140、SORBITAN、ISOSTEARATE、POLYSORBATE 60、BUTYLENEGLYCOL、1,2-HEXANEDIOL、DISODIUM EDTA、PVM/MA COPOLYMER、IODOPROPYNYL BUTYLCARBAMATE、CI 16255、PEG-90M

WARNINGS

Warning.
1.Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2、For external use only, avoid contact with eyes when used
3、Keep out of reach of children

INDICATIONS & USAGE

Triple action
-Moisturizer
-Dark spots remover
-Skin refining
Nano glutathione

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN SECTION

ACTIVE INGREDIENT

Active Ingredients
GLUTATHIONE 0.8%
KOJIC DIPALMITATE 1.3%
ASCORBIC ACID 0.3%

DOSAGE & ADMINISTRATION

a complexion
clarifying milk serum that removes and
fades out stubborn dark spots, acne scars,
sun spots and blemishes. It is a fast acting
milk serum that helps restore a clearer and
more radiant even-toned complexion while
also smoothing out dry skin.

PRINCIPAL DISPLAY PANEL

Active Ingredients
GLUTATHIONE 0.8%
KOJIC DIPALMITATE 1.3%
ASCORBIC ACID 0.3%

Uses：
For facial whitening
Indications: For facial whitening
The storage method：
Store sealed in a cool place and out of sunlight

Warning.
1.Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2、For external use only, avoid contact with eyes when used
3、Keep out of reach of children

Inactive ingredients：
AQUA、PROPYLENE GLYCOL、GLYCERETH-26、PENTAERYTHRITYL、TETRAETHYLHEXANOATE、ETHYLHEXYL PALMITATE、GLYCERIN、CETEARYL ALCOHOL、HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE、COPOLYMER、DMDM HYDANTOIN、XANTHAN GUM、CETEARYL GLUCOSIDE、AROMA、GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER、CI 19140、SORBITAN、ISOSTEARATE、POLYSORBATE 60、BUTYLENEGLYCOL、1,2-HEXANEDIOL、DISODIUM EDTA、PVM/MA COPOLYMER、IODOPROPYNYL BUTYLCARBAMATE、CI 16255、PEG-90M

INGREDIENTS AND APPEARANCE

5 DAYS WHITENING BOOSTER 
5 days whitening booster liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84423-017
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O)	GLUTATHIONE	0.8 mg  in 100 mg
KOJIC DIPALMITATE (UNII: 13N249RWTM) (KOJIC DIPALMITATE - UNII:13N249RWTM)	KOJIC DIPALMITATE	1.3 mg  in 100 mg
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	0.3 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
GLYCERETH-26 (UNII: NNE56F2N14)
XANTHAN GUM (UNII: TTV12P4NEE)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
1,4-BUTANEDIOL (UNII: 7XOO2LE6G3)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER (300000 CP AT 2%) (UNII: MEA9KH24QG)
POLYSORBATE 60 (UNII: CAL22UVI4M)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
PONCEAU 4R (UNII: Z525CBK9PG)
POLYETHYLENE GLYCOL 4000000 (UNII: RU64142H6P)
PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
METHYL VINYL ETHER AND MALEIC ANHYDRIDE COPOLYMER (1100000 WAMW) (UNII: T0VRI38HB0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84423-017-01	100 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	07/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/09/2024

Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Kadiya Biotechnology Co., Ltd.		713172913	manufacture(84423-017)