TOURCIA BODY WASH - allantoin solution 
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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Drug Facts

ACTIVE INGREDIENT

Active ingredient: ALLANTOIN 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
WATER, SODIUM LAURETH SULFATE, SODIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, COCAMIDE DEA, GLYCOL STEARATE, LAURAMIDE DEA, DISODIUM COCOAMPHODIACETATE, POLYQUATERNIUM-7, BUTYLENE GLYCOL, STEARYL ALCOHOL, SODIUM HYALURONATE, GLYCERIN, FRAGRANCE, CITRIC ACID, CETYL ETHYLHEXANOATE, ROYAL JELLY EXTRACT, 1,2-HEXANEDIOL , HAMAMELIS VIRGINIANA (WITCH HAZEL) WATER’, POLYQUATERNIUM-10, CORNUS OFFICINALIS FRUIT EXTRACT, SCHIZANDRA CHINENSIS FRUIT EXTRACT’ PUNICA GRANATUM FRUIT EXTRACT, ACACIA SEYAL GUM EXTRACT, BUTYROSPERMUM PARKII (SHEA) BUTTER, TOCOPHERYL ACETATE, DISODIUM EDTA, TOURMALINE, GELATIN

PURPOSE

PURPOSE: BODYWASH

WARNINGS

WARNINGS:
Do not apply the product to any area with abnormalities such as the area with scars, eczema, dermatitis

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN:
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER

INDICATIONS & USAGE

INDICATION AND USAGE:
After put the suitable amount on bath sponge or towel and foam sufficiently, apply it on the whole body like massage. Then, wash out completely.

DOSAGE & ADMINISTRATION

DOSAGE AND ADMINISTRATION:
Use as daily body wash. take 2-3 drops and apply on the body skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

TOURCIA BODY WASH 
allantoin solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43275-120
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN1.9 mg  in 380 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
GLYCOL STEARATE (UNII: 0324G66D0E)  
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GLYCERIN (UNII: PDC6A3C0OX)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)  
ROYAL JELLY (UNII: L497I37F0C)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
WITCH HAZEL (UNII: 101I4J0U34)  
CORNUS OFFICINALIS FRUIT (UNII: 23NL8NQ187)  
SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)  
POMEGRANATE (UNII: 56687D1Z4D)  
GUM TALHA (UNII: H18F76G097)  
SHEA BUTTER (UNII: K49155WL9Y)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GELATIN (UNII: 2G86QN327L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43275-120-01380 mL in 1 CARTON; Type 0: Not a Combination Product09/01/201112/31/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34709/01/201112/31/2013
Labeler - Nuga Medical Co.,Ltd. (690034673)
Registrant - Nuga Medical Co.,Ltd. (690034673)
Establishment
NameAddressID/FEIBusiness Operations
Nuga Medical Co.,Ltd.690034673manufacture(43275-120)

Revised: 7/2017
 
Nuga Medical Co.,Ltd.