28 REMEDY AQUA BRIGHTENING PEELING- allantoin gel 
NoTS Co.,Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

Active Ingredient: Allantoin 0.05%

INACTIVE INGREDIENT

Inactive Ingredients:

Water, Cellulose, Ethoxydiglycol, 1,2-Hexanediol, Betaine, Arginine, Carbomer, Niacinamide, Tocopheryl Acetate, Bambusa Arundinacea Stem Extract, Bisabolol, Betula Alba Juice, Salix Alba (Willow) Bark Extract, Lactobacillus/Soybean Ferment Extract, Portulaca Oleracea Extract, Origanum Vulgare Leaf Extract, Cinnamomum Cassia Bark Extract, Scutellaria Baicalensis Root Extract, Chamaecyparis Obtusa Leaf Extract, Ascorbic Acid

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings:

Stop use and ask dermatologist or doctor if

•signs of redness, skin swelling, itchy spots, irritation or rash and other appear

•the above signs appear in the applied area by direct rays of the sun

Do not use over

•wounds rashes inflammations other troubled areas.

When using

•Avoid the eye area

•must close the cap after using

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN:

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses: Exfoliate and hydrate skin

Directions

Directions:

•Dispense appropriate amount on your hand

•Apply appropriate amount over your face

•Gently massage the whole face until skin residue is visible then rinse thoroughly

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

28 REMEDY AQUA BRIGHTENING PEELING 
allantoin gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69716-090
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin0.05 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Alcohol (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69716-090-01100 mL in 1 CARTON; Type 0: Not a Combination Product01/02/201612/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/02/201612/01/2018
Labeler - NoTS Co.,Ltd (689004599)
Registrant - NoTS Co.,Ltd (689004599)
Establishment
NameAddressID/FEIBusiness Operations
Nowcos.Co.,Ltd689914984manufacture(69716-090)

Revised: 12/2018
 
NoTS Co.,Ltd