TOURCIA NUTRI EMULSION- 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, Glycerin, Butylene Glycol, Cyclopentasiloxane, Hydrogenated Poly(C6-14 Olefin), Trehalose, Polysorbate 60, Dimethicone, ALLANTOIN, Cetearyl Alcohol, Stearic Acid, Silica, Sorbitan Stearate, Glyceryl Stearate, PEG-100 Stearate, Phenoxyethanol, Methylparaben, Carbomer, Triethanolamine, Fragrance(Parfum), Propylparaben, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Dipotassium Glycyrrhizate, Tocopheryl Acetate, Isohexadecane, Adenosine, Disodium EDTA, Polysorbate 80, Sodium Cocoyl Alaninate, Caramel, Tourmaline, Propylene Glycol, Hydrolyzed Myrtus Communis Leaf Extract, Acacia Seyal Gum Extract, Gelatin, PVP, Potassium Sorbate, Ethylhexylglycerin, Butylparaben, Ethylparaben, Isobutylparaben, 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 it evenly to the skin after washing your face.

DOSAGE AND ADMINISTRATION

HOW TO USE:
Take a proper amount of this product and apply it evenly to the skin after washing your face.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

Image of carton

TOURCIA NUTRI EMULSION 
allantoin cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43275-160
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.65 mg  in 130 mL
Inactive Ingredients
Ingredient Name Strength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Trehalose (UNII: B8WCK70T7I)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43275-160-01 130 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(43275-160)

Revised: 2/2013
Document Id: ea39ac03-64cf-40fe-ac09-2fcb98522cdb
Set id: 16648e72-b657-48e5-9451-0ef5468cd7dd
Version: 1
Effective Time: 20130213
 
NUGA MEDICAL CO., LTD.