ZNSP REPAIR- glycerin cream 
Z-TON ES BIO CO., LTD.

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.

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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

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)

Revised: 6/2016
Document Id: e740a820-0096-4cb2-ab65-68a2ab858c4d
Set id: db887b99-5516-4754-8df5-ddca082d9a17
Version: 1
Effective Time: 20160602
 
Z-TON ES BIO CO., LTD.