Label: HOUKEA ORTHO CREAM- allantoin cream

  • NDC Code(s): 84660-080-01
  • Packager: Guangdong Ximonth Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2024

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  • Active Ingredient(s)

    MENTHA PIPERITA LEAF、SHEA BUTTER、TOCOPHEROL

  • Purpose

    Improves mobility

  • Use

    Take an appropriate amount of this product and apply it evenly on joints such as knees and elbows, and massage until absorbed.

  • 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

    GLYCERIN、ALLANTOIN

  • DOSAGE & ADMINISTRATION

  • INDICATIONS & USAGE

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    HOUKEA ORTHO CREAM 
    allantoin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84660-080
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL10 g  in 100 g
    SHEA BUTTER (UNII: K49155WL9Y) (SHEA BUTTER - UNII:K49155WL9Y) SHEA BUTTER15 g  in 100 g
    MENTHA PIPERITA LEAF (UNII: A389O33LX6) (MENTHA PIPERITA LEAF - UNII:A389O33LX6) MENTHA PIPERITA LEAF20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z) 25 g  in 100 g
    GLYCERIN (UNII: PDC6A3C0OX) 30 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84660-080-01100 g in 1 BOX; Type 0: Not a Combination Product10/22/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/22/2024
    Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Ximonth Technology Co., Ltd.699436264manufacture(84660-080)
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