Otc - Active Ingredient
Glycerin, Niacinamide
Suria Whitening
FDA Label NDC 81479-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sun C&b for the product Suria Whitening (NDC 81479-005). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, dosage & administration, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water, etc
Otc - Purpose
Skin Protectant - Anti-Wrinkle, Whitening
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Apply a small amount of cream on the face and gently pat the skin.
Dosage & Administration
For external use only
Warnings
1. If any of the following Symptoms occur, Cease use immediately. Continued usage would exacerbate the
symptoms. If symptoms persist, consult a doctor.
1) During of after usage, if red spots appear or you suffer from welling or itching or any other abnormal
symptoms after direct exposure to sunlight, consult a doctor immediately.
2)Avoid usage on cuts and wounds.
3) Storage and usage precautions.
A) Keep it out of reach of children.
B) Avoid exposure to direct sunlight during storage.
Package Label.Principal Display Panel
Cream (Cream)
* Please review the disclaimer below.
