MULBERRY EMULSION (ALLANTOIN) LIQUID [CORPORATION SORISO]

MULBERRY EMULSION (ALLANTOIN) LIQUID [CORPORATION SORISO]
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NDC 69969-005-01
Set ID a98973e7-850c-441f-8b1d-71f9fed59c45
Category HUMAN OTC DRUG LABEL
Packager CORPORATION SORISO
Generic Name
Product Class
Product Number
Application Number PART347
  • ACTIVE INGREDIENT

    ALLANTOIN


  • INACTIVE INGREDIENT

    water, butylene glycol, mineral oil, shea butter, etc.

  • PURPOSE

    skin protectant


  • KEEP OUT OF REACH OF CHILDREN

    keep out or 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


  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    MULBERRY EMULSION 
    allantoin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69969-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69969-005-01130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34707/10/2015
    Labeler - CORPORATION SORISO (689515253)
    Registrant - CORPORATION SORISO (689515253)
    Establishment
    NameAddressID/FEIBusiness Operations
    CORPORATION SORISO689515253manufacture(69969-005)

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