TOURCIA NUTRI TONER- 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, Glycereth-26, Glycerin, Dipropylene Glycol, Alcohol Denat., PEG/PPG-17/6 Copolymer, Bis-PEG-18 Methyl Ether Dimethyl Silane, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Methylparaben, Arginine, Carbomer, Adenosine, Fragrance(Parfum), Disodium EDTA, Propylene Glycol, Butylene Glycol, Acacia Seyal Gum Extract, PVP, Potassium Sorbate, Sodium Cocoyl Alaninate, Tourmaline, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Butylparaben, Ethylparaben, Isobutylparaben, Propylparaben, Hydrolyzed Myrtus Communis Leaf Extract, Fullerenes, Gelatin, Ethylhexylglycerin

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 TONER 
allantoin cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43275-190
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.75 mg  in 150 mL
Inactive Ingredients
Ingredient Name Strength
Water (UNII: 059QF0KO0R)  
Glycereth-26 (UNII: NNE56F2N14)  
Glycerin (UNII: PDC6A3C0OX)  
Dipropylene Glycol (UNII: E107L85C40)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43275-190-01 150 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(43275-190)

Revised: 2/2013
Document Id: 4db8c870-92f3-4474-a28b-90057870454a
Set id: fc8531e8-4cf4-4d1d-829a-694acdc58e5f
Version: 1
Effective Time: 20130213
 
NUGA MEDICAL CO., LTD.