FDA.reportPublic FDA data

BARUBT DEWY UNIVERSAL TINTED MOISTURIZER

Manufacturer
Guangdong Youbaijia Cosmetic Industry Co., Ltd
Effective date
2024-11-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:51:06

Label at a glance#

ProductBARUBT DEWY UNIVERSAL TINTED MOISTURIZER
Active ingredientPOLYGONUM AVICULARE WHOLE, NIACINAMIDE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Polygonum Aviculare Extract 0.5%
Niacinamide 5%

INACTIVE INGREDIENT SECTION

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

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children. Do not swallow.

OTC - PURPOSE SECTION

moisturising and sunscreen

OTC - QUESTIONS SECTION

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

OTC - STOP USE SECTION

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

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

WARNINGS SECTION

For external use only.

INDICATIONS & USAGE SECTION

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 SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84712-038-02BARUBT DEWY UNIVERSAL TINTED MOISTURIZER50 mL in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84712-038BARUBT DEWY UNIVERSAL TINTED MOISTURIZER (DEWY UNIVERSAL TINTED MOISTURIZER) CREAM [GUANGDONG YOUBAIJIA COSMETIC INDUSTRY CO., LTD]11 package rows20250109_27f59e52-421d-8844-e063-6294a90ac7c2.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84712-03884712-038-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOPENTASILOXANE0THT5PCI0RIACT
POLYGONUM AVICULARE WHOLEM990N03611ACTIB
NIACINAMIDE25X51I8RD4ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
27f59e52-421e-8844-e063-6294a90ac7c227f59e52-421d-8844-e063-6294a90ac7c22024-11-28WarningsExact identifier
spl id: 27f59e52-421e-8844-e063-6294a90ac7c2
spl set id: 27f59e52-421d-8844-e063-6294a90ac7c2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.