BARUBT GLUTA WHITENING LAZY CREAM- gluta whitening lazy cream cream

BARUBT Gluta Whitening Lazy Cream by

Drug Labeling and Warnings

BARUBT Gluta Whitening Lazy Cream by is a Otc medication manufactured, distributed, or labeled by Guangdong Youbaijia Cosmetic Industry Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ALLANTOIN 0.1%
3-o-ETHYL ASCORBIC ACID 0.1%
HIPPOPHAE RHAMNOIDES FRUIT JUICE 0.01%

INACTIVE INGREDIENT

WATER. GLYCERIN, MINERAL OIL, ETHYLHEXYL PALMITATE, TITANIUM DIOXIDE. GLYCERYL GLUCOSIDE.DIMETHICONE, POLYACRYLAMIDE, PHENOXYETHANOL, C13-14 ISOPARAFFIN. CETEARYL GLUCOSIDE, PEG-20 METHYL GLUCOSE SESQUISTEARATE. METHYLPARABEN, METHYL GLUCOSE SESQUISTEARATE. CETEARYL ALCOHOL, GLYCERYL STEARATE, PROPYLPARABEN. PARFUM, LAURETH-7, ALUMINA. TRIETHOXYCAPRYLYLSILANE. CETEARETH-25, AQUA. ETHYLHEXYLGLYCERIN. TREMELLA FUCIFORMIS POLYSACCHARIDE, GLUTAMINE. 1,2-HEXANEDIOL, HYDROXYACETOPHENONE.

DO NOT USE

on damaged or broken skin

KEEP OUT OF REACH OF CHILDREN

Keep away from children. Do not swallow.

PURPOSE

WHITENS AND BRIGHTENS THE SKIN

QUESTIONS

Contact name: Jessie Peng
Company phone number: +1 818 579 7288
Company e-mail: jessie@registeragentllc.com

STOP USE

lf skin becomes red or irritated, discontinue use immediately and wash with water.

WHEN USING

keep out of eyes. Rinse with water to remove.

INDICATIONS & USAGE

WHITENS AND BRIGHTENS THE SKIN, EFFECTIVELY INHIBITS MELANIN, BLOCKS MELANIN TRANSFER, HAS ANTIOXIDANT FUNCTION, WAKE UP BRIGHT AND SMOOTH SKIN

DOSAGE & ADMINISTRATION

CLEANSE AND DRY THE SKIN APPLY THE CREAM TO THE FACE AND MASSAGE UNTIL FULLY ABSORBED. UNTIL FULLY ABSORBED. FOR BEST RESULTS, USE TWICE A DAY, ONCE IN THE MORNING AND ONCE IN THE EVENING.

WARNINGS

For external use only.

STORAGE AND HANDLING

Keep away from light and in a dry place.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BARUBT GLUTA WHITENING LAZY CREAM 
gluta whitening lazy cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84712-033
Route of Administration	TOPICAL, CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) (3-O-ETHYL ASCORBIC ACID - UNII:6MW60CB71P)	3-O-ETHYL ASCORBIC ACID	0.03 g  in 30 g
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.03 g  in 30 g
HIPPOPHAE RHAMNOIDES FRUIT JUICE (UNII: UC3P08EB3Y) (HIPPOPHAE RHAMNOIDES FRUIT JUICE - UNII:UC3P08EB3Y)	HIPPOPHAE RHAMNOIDES FRUIT JUICE	0.003 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)	1.2 g  in 30 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84712-033-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/27/2024

Labeler - Guangdong Youbaijia Cosmetic Industry Co., Ltd (702314361)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Youbaijia Cosmetic Industry Co., Ltd		702314361	label(84712-033) , manufacture(84712-033)