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ZNSP Ampoule

Medically reviewed on June 4, 2018

Dosage form: solution
Ingredients: GLYCERIN 0.25g in 5mL
Labeler: Z-TON ES BIO CO., LTD.
NDC Code: 70749-010

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.

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

ZNSP AMPOULE 
glycerin solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70749-010
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN0.25 g  in 5 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
METHYLPROPANEDIOL 
Packaging
#Item CodePackage Description
1NDC:70749-010-0215 BOTTLE in 1 CARTON
1NDC:70749-010-015 mL in 1 BOTTLE
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/FEIOperations
Z-TON ES BIO CO., LTD.689847169manufacture(70749-010)

 
Z-TON ES BIO CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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