ULTRA SOOTHING TONER (ALLANTOIN) LIQUID [DERMAFIRM INC.]

ULTRA SOOTHING TONER (ALLANTOIN) LIQUID [DERMAFIRM INC.]
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NDC 71638-0008-1
Set ID 58569429-5db2-3bcb-e053-2a91aa0abb87
Category HUMAN OTC DRUG LABEL
Packager Dermafirm INC.
Generic Name
Product Class
Product Number
Application Number PART347
  • ACTIVE INGREDIENT

    Allantoin

  • INACTIVE INGREDIENT

    Water, Glycerin

  • PURPOSE

    Skin protectant

    Soothing

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    After cleansing, soak it in a cotton swab and use it as if you wipe it out carefully.

  • 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

    label

  • INGREDIENTS AND APPEARANCE
    ULTRA SOOTHING TONER 
    allantoin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71638-0008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71638-0008-1200 mL in 1 BOTTLE; Type 0: Not a Combination Product09/04/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34709/04/2017
    Labeler - Dermafirm INC. (690171603)
    Registrant - Dermafirm INC. (690171603)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dermafirm INC.690171603label(71638-0008) , pack(71638-0008) , manufacture(71638-0008)

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