Label: HUCORD HSCM-100 AMPOULE- insulin-like growth factor-2 liquid

  • 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 December 23, 2019

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  • ACTIVE INGREDIENT

    dimethicone


  • INACTIVE INGREDIENT

    water, butylene glycol, etc.


  • PURPOSE

    anti aging


  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children


  • INDICATIONS & USAGE

    apply proper amount to the skin


  • WARNINGS

    1. Do not use in the following cases(Eczema and scalp wounds)
    2.Side Effects
    1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
    3.General Precautions
    1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
    2)This product is for exeternal use only. Do not use for internal use
    4.Storage and handling precautions
    1)If possible, avoid direct sunlight and store in cool and area of low humidity
    2)In order to maintain the quality of the product and avoid misuse
    3)Avoid placing the product near fire and store out in reach of children

  • DOSAGE & ADMINISTRATION

    for external use only


  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    HUCORD HSCM-100 AMPOULE 
    insulin-like growth factor-2 liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70373-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    INSULIN-LIKE GROWTH FACTOR-2 (UNII: 95067D43FQ) (DIMETHICONE - UNII:92RU3N3Y1O) INSULIN-LIKE GROWTH FACTOR-20.0000633 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    INTERLEUKIN-8 (UNII: PC30892LX5)  
    HUMAN EPIDERMAL GROWTH FACTOR (UNII: TZK30RF92W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70373-0003-112 mL in 1 PACKAGE; Type 0: Not a Combination Product12/29/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/29/2015
    Labeler - Hucord Co., Ltd. (688013812)
    Registrant - Hucord Co., Ltd. (688013812)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hucord Co., Ltd.688013812manufacture(70373-0003)