7 DAYS WHITENING FACE CREAM cream

7 Days Whitening Face Cream by

Drug Labeling and Warnings

7 Days Whitening Face Cream by is a Otc medication manufactured, distributed, or labeled by Guangzhou Kadiya Biotechnology Co.,,Ltd., Guangzhou Kadiya Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGEDIENT

GLUTATHIONE 0.5%
ALPHA-ARBUTIN 1%
ALOE BARBADENSIS1.25%

PURPOSE

For Face Whitening and Hydrating

INACTIVE INGREDIENT

AQUA, GLYCERIN, MINERAL OIL, HYDROXYACETOPHENONE, 1,2-HEXANEDIOL,BUTYLENE GLYCOL, PALMITIC ACID, STEARIC ACID, MYRISTIC ACID, LAURIC ACID, DIMETHICONE, NIACINAMIDE, GLYCERYL STEARATE, POLYSORBATE 60, Water, BUTYLENE GLYCOL, ANTHEMIS NOBILIS FLOWER EXTRACT, PORTULACA OLERACEA FLOWER/LEAF/STEM EXTRACT, PELARGONIUM GRAVEOLENS FLOWER/LEAF/STEM EXTRACT, STEARYL ALCOHOL, CETYL ALCOHOL, TRANEXAMIC ACID, TITANIUM DIOXIDE, ALUMINA, TRIETHANOLAMINE, PEG-75 LANOLIN, PHENOXYETHANOL, ALLANTOIN, METHYLPARABEN, PROPYLPARABEN, CI 19140, SODIUM CHLORIDE, CI 15985.

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

INSTRUCTIONS FOR USE

Before using this Day Face Cream, Kindly remove all the impurities from your face. Apply and massage for sometimes.

INDICATIONS

Before using this Day Face Cream, Kindly remove all the impurities from your face. Apply and massage for sometimes. The first result can be seen after 7 days.

DOSAGE

For external use only, avoid contact with eyes when used

WARNING

keep out of reach of children

PRINCIPAL DISPLAY PANEL

7 DAYS WHITENING FACE CREAM

1. Active Ingredients
GLUTATHIONE 0.5%
ALPHA-ARBUTIN 1%
ALOE BARBADENSIS1.25%

2.Purpose
For Face Whitening and Moisturizing

3.Inactive ingredients:
AQUA, GLYCERIN, MINERAL OIL, HYDROXYACETOPHENONE, 1,2-HEXANEDIOL,BUTYLENE GLYCOL, PALMITIC ACID, STEARIC ACID, MYRISTIC ACID, LAURIC ACID, DIMETHICONE, NIACINAMIDE, GLYCERYL STEARATE, POLYSORBATE 60, Water, BUTYLENE GLYCOL, ANTHEMIS NOBILIS FLOWER EXTRACT, PORTULACA OLERACEA FLOWER/LEAF/STEM EXTRACT, PELARGONIUM GRAVEOLENS FLOWER/LEAF/STEM EXTRACT, STEARYL ALCOHOL, CETYL ALCOHOL, TRANEXAMIC ACID, TITANIUM DIOXIDE, ALUMINA, TRIETHANOLAMINE, PEG-75 LANOLIN, PHENOXYETHANOL, ALLANTOIN, METHYLPARABEN, PROPYLPARABEN, CI 19140, SODIUM CHLORIDE, CI 15985.

4.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

INGREDIENTS AND APPEARANCE

7 DAYS WHITENING FACE CREAM 
7 days whitening face cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84423-006
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5)	ALPHA-ARBUTIN	0.5 mg  in 50 mg
GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O)	GLUTATHIONE	0.25 mg  in 50 mg
ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X)	ALOE VERA LEAF	0.625 mg  in 50 mg

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
PELARGONIUM GRAVEOLENS FLOWERING TOP (UNII: 1P36QZP48P)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ALUMINUM OXIDE (UNII: LMI26O6933)
PALMITIC ACID (UNII: 2V16EO95H1)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
NIACINAMIDE (UNII: 25X51I8RD4)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETYL ALCOHOL (UNII: 936JST6JCN)
LAURIC ACID (UNII: 1160N9NU9U)
ALLANTOIN (UNII: 344S277G0Z)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
TRANEXAMIC ACID (UNII: 6T84R30KC1)
MINERAL OIL (UNII: T5L8T28FGP)
PURSLANE (UNII: M6S840WXG5)
PEG-75 LANOLIN (UNII: 09179OX7TB)
METHYLPARABEN (UNII: A2I8C7HI9T)
STEARIC ACID (UNII: 4ELV7Z65AP)
MYRISTIC ACID (UNII: 0I3V7S25AW)
POLYSORBATE 60 (UNII: CAL22UVI4M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84423-006-01	50 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	07/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/01/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Kadiya Biotechnology Co., Ltd.		713172913	manufacture(84423-006)