ZNSP REPAIR- glycerin cream

ZNSP Repair by

Drug Labeling and Warnings

ZNSP Repair by is a Otc medication manufactured, distributed, or labeled by Z-TON ES BIO CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

ZNSP REPAIR 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70749-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.16 g  in 8 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70749-020-02	10 in 1 CARTON	05/01/2016
1	NDC: 70749-020-01	8 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2016

Labeler - Z-TON ES BIO CO., LTD. (689847169)

Registrant - Z-TON ES BIO CO., LTD. (689847169)

Establishment
Name	Address	ID/FEI	Business Operations
Z-TON ES BIO CO., LTD.		689847169	manufacture(70749-020)