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

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.75 mg in 150 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Glycereth-26 (UNII: NNE56F2N14)
Glycerin (UNII: PDC6A3C0OX)
Dipropylene Glycol (UNII: E107L85C40)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43275-190-01	150 mL in 1 CARTON; Type 0: Not a Combination Product	10/01/2012	12/31/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	10/01/2012	12/31/2013

Labeler - Nuga Medical Co.,Ltd. (690034673)

Registrant - Nuga Medical Co.,Ltd. (690034673)

Name	Address	ID/FEI	Business Operations
Establishment
Nuga Medical Co.,Ltd.		690034673	manufacture(43275-190)

Revised: 8/2017

Document Id: 6369b7af-4db7-476a-b845-b99276e2c0d6

Set id: fc8531e8-4cf4-4d1d-829a-694acdc58e5f

Version: 2

Effective Time: 20170801

Nuga Medical Co.,Ltd.