BARUBT DEWY UNIVERSAL TINTED MOISTURIZER- dewy universal tinted moisturizer cream

BARUBT DEWY UNIVERSAL TINTED MOISTURIZER by

Drug Labeling and Warnings

BARUBT DEWY UNIVERSAL TINTED MOISTURIZER 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

Polygonum Aviculare Extract 0.5%
Niacinamide 5%

INACTIVE INGREDIENT

Water/Aqua/Eau, Cyclopentasiloxane, Oleth-3 Phosphate, Octyldodecyl Neopentanoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glycerin, Sodium Hyaluronate, Tocopheryl Acetate, Ethylhexylglycerin, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, PEG-7 Trimethylolpropane Coconut Ether, Polyisobutene, Triethoxycaprylylsilane, Disodium EDTA, Iron Oxides, Phenoxyethanol

DO NOT USE

Do not use on damaged or broken skin

KEEP OUT OF REACH OF CHILDREN

Keep away from children. Do not swallow.

PURPOSE

moisturising and sunscreen

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

WHEN USING

keep out of eyes. Rinse with water to remove.

WARNINGS

For external use only.

INDICATIONS & USAGE

This moisturiser combines sun protection and lightweight tinted coverage to naturally match skin colour. The lightweight, moisturising texture nourishes dry skin for long-lasting hydration, while the SPF 46 broad-spectrum sunscreen protects against the sun's harmful effects.

DOSAGE & ADMINISTRATION

Apply to face and neck, avoiding the eye area.Wait at least 30 minutes before sunbathing. Reapply after prolonged sun exposure, exercise, sweating or contactwith water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BARUBT DEWY UNIVERSAL TINTED MOISTURIZER 
dewy universal tinted moisturizer cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84712-038
Route of Administration	CUTANEOUS, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYGONUM AVICULARE WHOLE (UNII: M990N03611) (POLYGONUM AVICULARE WHOLE - UNII:M990N03611)	POLYGONUM AVICULARE WHOLE	0.25 g  in 50 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2.5 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)	4 g  in 50 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84712-038-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/28/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Youbaijia Cosmetic Industry Co., Ltd		702314361	label(84712-038) , manufacture(84712-038)