Label: ZNSP REPAIR- glycerin cream

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

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 June 2, 2016

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredient: GLYCERIN 2.0%

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Butylene Glycol, Methyl Gluceth-20, Human Stem Cell Conditioned Media, Hydroxyethylcellulose, Carbomer, Triethanolamine, Saccharomyces/Viscum Album (Mistletoe) Ferment Extract, Saccharomyces/Imperata Cylindrica Root Ferment Extract, Lactobacillus/Soybean Ferment Extract, Chlorphenesin, Phenoxyethanol, Allantoin, Aloe Barbadensis Leaf Extract, Camellia Sinensis Leaf Extract, Sodium Hyaluronate, Disodium EDTA, Dipotassium Glycyrrhizate

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: 1. It is recommend stopping applying and consulting 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. After treatment and in case of irritation, apply an appropriate amount on the skin and help the penetration with massage.

  • DOSAGE & ADMINISTRATION

    Dosage & Administration:

    Apply 2ml per each time, gently wrap your skin to help an absorption

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    ZNSP REPAIR 
    glycerin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70749-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.16 g  in 8 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70749-020-0210 in 1 CARTON05/01/2016
    1NDC:70749-020-018 g 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(70749-020)