Label: DR.PAUHLS NATURAL TONE UP TOOTH- hydrogen peroxide solution, colloidal silicon dioxide, tocopherol acetate paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 72265-100-01, 72265-100-02 - Packager: CURESCRIPT
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 9, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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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
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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
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.PAUHLS NATURAL TONE UP TOOTH
hydrogen peroxide solution, colloidal silicon dioxide, tocopherol acetate paste, dentifriceProduct 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)
