Label: ZNSP AMPOULE- glycerin solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 2, 2016

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  • ACTIVE INGREDIENT

    Active Ingredient: GLYCERIN 5.0%

  • INACTIVE INGREDIENT

    Inactive Ingredients: WATER, ACETYL HEXAPEPTIDE-8, Methyl PROPANDIOL, ARBUTINE, CITRUSPARADISI(GRAPEFRUIT)FRUIT EXTRACT, SCUTELLARIA BAICALENSISROOT EXTRACT, PAEONIA SUFFRUTICOSAROOT EXTRACT, 1,2-HEXANDIOL, SODIUM HYALURONATE, CARBOMER, ADENOSINE, DISODIUM EDTA

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: 1. It is recommended to stop applying and consult a doctor immediately if you are suffering such conditions A) In case of rash, swell-up, itchiness B) If applied part is suffering conditions above on direct exposure to sunlight 2. Do not apply directly to wound or open cut 3. Cautions on storage A) Keep the cap sealed B) Away from children C) Do not leave it on high, low temperature or exposed on sunlight

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS & USAGE

    Indications & usage: 1. Carefully open the ampoule

    2-1. Without compressor: Apply an appropriate amount of the product on the clean face skin. Gently smooth over entire face to help the absorption of the product.

    2-2. With compressor: insert one ampoule into compressor and gently spray it all over the face.

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: Apply 2ml per each time; gently wrap your skin to help absorption

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    image of carton

  • INGREDIENTS AND APPEARANCE
    ZNSP AMPOULE 
    glycerin solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70749-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.25 g  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70749-010-0215 in 1 CARTON05/01/2016
    1NDC:70749-010-015 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2016
    Labeler - Z-TON ES BIO CO., LTD. (689847169)
    Registrant - Z-TON ES BIO CO., LTD. (689847169)
    Establishment
    NameAddressID/FEIBusiness Operations
    Z-TON ES BIO CO., LTD.689847169manufacture(70749-010)
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