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

DR.PAUHLS NATURAL TONE UP TOOTH by

Drug Labeling and Warnings

DR.PAUHLS NATURAL TONE UP TOOTH by is a Otc medication manufactured, distributed, or labeled by CURESCRIPT, Sungwon Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72265-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	1.81 g  in 85 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	5.95 g  in 85 g
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1)	.ALPHA.-TOCOPHEROL ACETATE	0.17 g  in 85 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72265-100-02	1 in 1 CARTON	02/01/2021
1	NDC: 72265-100-01	85 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/01/2021

Labeler - CURESCRIPT (694894509)

Registrant - CURESCRIPT (694894509)

Establishment
Name	Address	ID/FEI	Business Operations
Sungwon Pharmaceutical Co., Ltd.		689787898	manufacture(72265-100)