BARUBT BRIGHTENING- brightening cream

BARUBT BRIGHTENING by

Drug Labeling and Warnings

BARUBT BRIGHTENING 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 Ingredients

glucoside ascorbate 1%

niacin 0.6%

NIACINAMIDE 0.05%

Purpose

whitening and freckle removing, brightening skin

Uses

After cleansing, apply to face and massage until completely absorbed.

Warnings

For external use only. Keep out of the reach of children.Avoid contact with eyes.

Stop use

Discontinue use if signs of irritation or rash occur.

Do not use

on damaged or broken skin

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

When using this product

keep out of eyes. Rinse with water to remove

DOSAGE & ADMINISTRATION

• well cleansing your face
• apply mean brightening cream to face and massage until completely absorbed.
• children under 6 months ofage: Ask a doctor

Inactive ingredient

Water
polydimethylsiloxane
caprylic acid/Caprylic acid triglyceride
Mineral Oil
Propylene glycol
stearin-2
Glycerin stearate
cetyl alcohol
stearin-21
Red myrrh alcohol
bis(hydroxymethyl) imidazolidinyl Urea
hydroxyphenylate
hydroxypropyl ester
Essence

Storage and handling

Store in a cool and dry place.

Questions

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BARUBT BRIGHTENING 
brightening cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84712-001
Route of Administration	TOPICAL, CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.01 g  in 20 g
NIACIN (UNII: 2679MF687A) (NIACIN - UNII:2679MF687A)	NIACIN	0.12 g  in 20 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	14.768 g  in 20 g
MINERAL OIL (UNII: T5L8T28FGP)	0.7 g  in 20 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84712-001-01	20 g in 1 BOTTLE; Type 0: Not a Combination Product	09/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/05/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Youbaijia Cosmetic Industry Co., Ltd		702314361	manufacture(84712-001) , label(84712-001)