DR.PAUHLS NATURAL TONE UP TOOTH- hydrogen peroxide solution, colloidal silicon dioxide, tocopherol acetate paste, dentifrice 
CURESCRIPT

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 INGREDIENTS

Hydrogen Peroxide Solution (35%) 2.14 %
Colloidal silicon dioxide 7.0%
Tocopherol Acetate 0.2%

INACTIVE INGREDIENTS

D-Sorbitol Solution, Deionized Water , Glycerin ,Carboxymethylcellulose Sodium ,Sodium Cocoyl Glutamate ,Sodium Lauroyl Sarcosinate ,Grapefruit Seed Extract ,Enzymatically Modified Stevia ,Xylitol ,Xanthan Gum ,Melon champagne Flavor ,Citric Acid ,L-Menthol ,Mentha Oil ,Spearmint oil ,Polysorbate 60,Hydroxyapatite ,Eucalyptus Oil,Parsley Extract ,Salicylic Acid,Clove Oil

PURPOSE

Whitening
Anti plaque
prevent gingivitis

WARNINGS

■ Do not use for any other purposes except brushing your teeth.
■ Do not swallow, and rinse your mouth adequately after use.
■ Consult your physician or dentist and follow their directions if you swallow a large amount of toothpaste.
■ Discontinue use and consult your physician or dentist if gum or mouth pain occurs after using this toothpaste
■ Keep out of reach of children and guide them if they use this toothpaste.
■ Store it away from high or low temperature and from direct sunlight.

KEEP OUT OF REACH OF CHILDREN

■ Keep out of reach of children and guide them if they use this toothpaste.

Uses

■ Promotes dental health and removal bad breath, makes tooth bright

Directions

■ Brush the teeth with a suitable amount.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

DR.PAUHLS NATURAL TONE UP TOOTH 
hydrogen peroxide solution, colloidal silicon dioxide, tocopherol acetate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72265-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE1.81 g  in 85 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE5.95 g  in 85 g
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE0.17 g  in 85 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL (UNII: 506T60A25R)  
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72265-100-021 in 1 CARTON02/01/2021
1NDC:72265-100-0185 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/01/2021
Labeler - CURESCRIPT (694894509)
Registrant - CURESCRIPT (694894509)
Establishment
NameAddressID/FEIBusiness Operations
Sungwon Pharmaceutical Co., Ltd.689787898manufacture(72265-100)

Revised: 2/2021
Document Id: 387db461-f3c7-42d6-92f3-5b16468e98f5
Set id: 3614aea9-9897-41de-8744-ef640df7c062
Version: 1
Effective Time: 20210209
 
CURESCRIPT