Active Ingredients
glucoside ascorbate 1%
niacin 0.6%
NIACINAMIDE 0.05%
Barubt Brightening
FDA Label NDC 84712-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Youbaijia Cosmetic Industry Co., Ltd for the product Barubt Brightening (NDC 84712-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, stop use, do not use, keep out of reach of children, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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: [email protected]
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