Label: JAYSUING SNOW BLEACH CREAM- allantoin cream

  • NDC Code(s): 84660-024-01
  • Packager: Guangdong Ximonth Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 24, 2024

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  • Active Ingredient(s)

    GLUTATHIONE, CENTELLA ASIATICA EXTRACT,ASCORBIC ACID,NIACINAMIDE, CHAMOMILLA RECUTITA(MATRICARIA) FLOWER EXTRACT

  • Purpose

    Elastic and smooth skin

  • Use

    1. Clean and dry skin
    2. Apply to skin until completely absorbed
    3. For best results, use twice aday in the morning and evening

  • Warnings

    Please keep out of reach of children.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place

  • Do not use

    Discontinue use if signs of irritation or rash occur

  • STOP USE

    Discontinue use if signs of irritation or rash occur

  • KEEP OUT OF REACH OF CHILDREN

    Please keep out of reach of children. Do not swallow.

  • STORAGE AND HANDLING

    Avoid freezing and excessive heat above 40C (104F) ）
    Store in a cool and dry place.

  • INACTIVE INGREDIENT

    ALLANTOIN

  • DOSAGE & ADMINISTRATION

  • INDICATIONS & USAGE

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    JAYSUING SNOW BLEACH CREAM 
    allantoin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84660-024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) (CENTELLA ASIATICA TRITERPENOIDS - UNII:4YS74Q4G4J) CENTELLA ASIATICA TRITERPENOIDS6 mg  in 30 mg
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE4.5 mg  in 30 mg
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID4.5 mg  in 30 mg
    GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE3 mg  in 30 mg
    CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X) CHAMOMILE3 mg  in 30 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z) 9 mg  in 30 mg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84660-024-0130 mg in 1 BOX; Type 0: Not a Combination Product09/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/24/2024
    Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Ximonth Technology Co., Ltd.699436264manufacture(84660-024)
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