Label: SURIA WHITENING cream

  • Category: HUMAN OTC DRUG LABEL

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 healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Glycerin, Niacinamide

  • INACTIVE INGREDIENT

    Water, etc

  • PURPOSE

    Skin Protectant - Anti-Wrinkle, Whitening

  • 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.

  • PRINCIPAL DISPLAY PANEL

    cream

  • INGREDIENTS AND APPEARANCE
    SURIA WHITENING 
    suria whitening cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81479-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 50 mL
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 46 g  in 50 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81479-005-0150 mL in 1 CONTAINER; Type 0: Not a Combination Product01/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2021
    Labeler - SUN C&B (695641205)
    Establishment
    NameAddressID/FEIBusiness Operations
    SUN C&B695641205manufacture(81479-005)