BRIGHT BOOST CREAM cream

Bright Boost Cream by

Drug Labeling and Warnings

Bright Boost Cream by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xiaomai Manufacturing Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Arbutin

PURPOSE

whiten skin

INDICATIONS

whiten skin

Warnings

Warnings

For external use only.

Do not use

Do not use on damaged or brokenskin.

When using this product

Wnen using tnis product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

Keep out of reach of children.

Directions for use

Use twice daily, in the morning and evening.
Apply an appropriate amount of cream evenly tothe cleansed face and neck.
Gently massage until fully absorbed.
Increase frequency of use as needed based onskin condition.

INACTIVE INGREDIENT

Arbutin
Aqua
Glycerin
Sodium Hyaluronate
Stearyl Alcohol
Propanediol
Hydrogenated Lecithin
Squalane
Retinol

Other Information

Store in a cool, dry place. "Avoid direct sunlight.
Consult a dermatologist if you have any questions.

label

INGREDIENTS AND APPEARANCE

BRIGHT BOOST CREAM 
bright boost cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83872-192
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF)	ARBUTIN	50 g  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
AQUA REGIA (UNII: X3TT5X989E)	600 g  in 1 mg
SQUALANE (UNII: GW89575KF9)	50 g  in 1 mg
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)	50 g  in 1 mg
22-HYDROGENATED RACEMIC CALCIPOTRIOL (UNII: 96516X6183)	10 g  in 1 mg
GLYCERIN (UNII: PDC6A3C0OX)	100 g  in 1 mg
2-AMINO-1,3-PROPANEDIOL (UNII: IC94L30J8M)	30 g  in 1 mg
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)	50 g  in 1 mg

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83872-192-01	50 mg in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/24/2024

Labeler - Shenzhen Xiaomai Manufacturing Co Ltd (712999147)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xiaomai Manufacturing Co Ltd		712999147	manufacture(83872-192)