TOURCIA NUTRI ESSENCE- allantoin cream 
NUGA MEDICAL CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

ACTIVE INGREDIENT: ALLANTOIN 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
Water, Butylene Glycol, Glycerin, Bis-PEG-18 Methyl Ether Dimethyl Silane, Dipropylene Glycol, PEG-75, Glycereth-26, Maltitol, Methyl Gluceth-20, Biosaccharide Gum-1, Yeast Extract, PEG-60 Hydrogenated Castor Oil, Phenoxyethanol, Silica, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Polymethylsilsesquioxane, Methylparaben, Ammonium Acryloyldimethyltaurate/VP Copolymer, Xanthan Gum, Caffeine, Caramel, Fragrance(Parfum), Bifida Ferment Lysate, Adenosine, Dipotassium Glycyrrhizate, Neopentyl Glycol Dicaprate, Cetyl Ethylhexanoate, Disodium EDTA, Sodium Chondroitin Sulfate, Ceteth-20, Steareth-20, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Leuconostoc/Radish Root Ferment Filtrate Sodium Hyaluronate, Tourmaline, Glyceryl Stearate, Cetearyl Alcohol, Propylene Glycol, Hydrolyzed Myrtus Communis Leaf Extract, Potassium Sorbate, Tocopheryl Acetate, Acacia Seyal Gum Extract Gelatin, Lactic Acid, Acetic Acid, Ethylhexylglycerin, PVP, Butylparaben, Ethylparaben, Isobutylparaben, Propylparaben, Sodium Cocoyl Alaninate, Fullerenes

PURPOSE

PURPOSE: Wrinkle Functional cosmetics (Skin Protectant)

WARNINGS

WARNINGS:
For external use only
Do Not Use - On wounds or damaged skin
When using this product:
- do not use other than directed
Stop use - If allergic reaction or irritation occurs

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

HOW TO USE:
Take a proper amount of this product and apply, absorb it softly to the skin.

DOSAGE AND ADMINISTRATION

HOW TO USE:
Take a proper amount of this product and apply, absorb it softly to the skin.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

Image of carton

TOURCIA NUTRI ESSENCE 
allantoin cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43275-170
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.15 mg  in 30 mL
Inactive Ingredients
Ingredient Name Strength
Water (UNII: 059QF0KO0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Glycerin (UNII: PDC6A3C0OX)  
Dipropylene Glycol (UNII: E107L85C40)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43275-170-01 30 mL in 1 CARTON
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part347 10/01/2012
Labeler - NUGA MEDICAL CO., LTD. (690034673)
Registrant - NUGA MEDICAL CO., LTD. (690034673)
Establishment
Name Address ID/FEI Business Operations
NUGA MEDICAL CO., LTD. 690034673 manufacture(43275-170)

Revised: 2/2013
Document Id: d9101e39-4c13-480e-8197-f01a6280161d
Set id: c8ae095a-f677-414c-973f-752a5face117
Version: 1
Effective Time: 20130213
 
NUGA MEDICAL CO., LTD.