Label: SURIA WHITENING cream
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Contains inactivated NDC Code(s)
NDC Code(s): 81479-005-01 - Packager: SUN C&B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 31, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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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. - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SURIA WHITENING
suria whitening creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81479-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 50 mL GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2 g in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 46 g in 50 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81479-005-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product 01/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2021 Labeler - SUN C&B (695641205) Establishment Name Address ID/FEI Business Operations SUN C&B 695641205 manufacture(81479-005)