Label: GENE 16 WHITENING FACTOR- allantoin tablet, soluble

  • NDC Code(s): 69764-001-10
  • Packager: Shanghai Liang Liang International Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 29, 2023

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  • Active Ingredient

    Allantoin 0.5%

  • Purpose

    Allantoin    Skin Lightener

                     Skin Protectant

  • Warning

    For External Use Only.

  • Use

    Apply moderate amount of the product on the skin.

  • Stop Using the Product if

    Stop using the product when you have skin problems or the product disagrees with your skin.
    ・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
    ・If the product gets into the eyes, don't rub but rinse with water.

  • Keep Out of Reach of Children

    Keep out of reach of children.

  • When Using the Product

    Mix one tablet with water in palm to dissolve before applying to skin. Two tablets two times a day. One after face cleanse in the morning; and one before bed.

  • Other Information

    Keep in a dry, cool place away from direct sunlight. Store at room temperature.

  • Contact the Manufacturer or Distributor

    Manufactured by Shanghai Liang Liang International Inc.
    No. 876, TaoGan Road, Sheshan Town, Songjiang District, Shanghai 201602, China
    (86)21-57794082

    Distributed by Shanghai Liang Liang International Inc (USA)

  • Inactive Ingredients

    HYALURONIC ACID, TREHALOSE, MANNITOL, GLYCYRRHIZA GLABRA, CENTELLA ASIATICA, RESVERATROL, ARBUTIN, NIACINAMIDE, LECITHIN SOYBEAN, CERAMIDE 3, TOCOPHEROL, ASTAXANTHIN, PUNICA GRANATUM WHOLE

  • Drug Facts

    product description

  • INGREDIENTS AND APPEARANCE
    GENE 16 WHITENING FACTOR 
    allantoin tablet, soluble
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69764-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.5 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    HYALURONIC ACID (UNII: S270N0TRQY)  
    TREHALOSE (UNII: B8WCK70T7I)  
    MANNITOL (UNII: 3OWL53L36A)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    CENTELLA ASIATICA (UNII: 7M867G6T1U)  
    RESVERATROL (UNII: Q369O8926L)  
    ARBUTIN (UNII: C5INA23HXF)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    CERAMIDE 3 (UNII: 4370DF050B)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ASTAXANTHIN (UNII: 8XPW32PR7I)  
    PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize8mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69764-001-101 in 1 PACKAGE09/25/2014
    17 mg in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/25/2014
    Labeler - Shanghai Liang Liang International Inc (547834726)
    Registrant - Shanghai Liang Liang International Inc (547834726)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shanghai Liang Liang International Inc547834726manufacture(69764-001)
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