Label: DR.LORD PROPOL WHITENING TOOTH- hydrogen peroxide, colloidal silicon dioxide, tocopherol acetate paste, dentifrice
- NDC Code(s): 82656-020-01, 82656-020-02
- Packager: Red 99
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 6, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Liquid sorbitol(Non-crystallising)(70%), Purified Water, Xylitol, Polyethylene Glycol 1500, Sodium Lauryl Sulfate, Zanthan gum, Polyvinylpyrrolidone K 30, CarboxymethylcelluloseSodium, Polyoxyethylene hydrogenated caster oil, Peppermint Flavor EM-16B196, Sodium Stannate, Phosphoric acid, Sodium Benzoate, Saccharin Sodium Hydrate, Calendula Flavor EM-16B015, Disodium dihydrogen diphosphate; Disodium, Menthol, Poloxamer 407, Polyvinyl alcohol, Spearmint Oil, Trisodium Citrate dehydrate, ethylenediaminetetraacetic acid EDTA, Citric Acid, Sodium Phosphate dibasic, Propolis Extract, Rosemary Oil
- PURPOSE
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WARNINGS
1. Application Precautions
1) Do not use it for anything other than brushing your teeth.
2) If you eat too much of this product, follow the instructions of a pharmacist, dentist, or doctor.
2. Storage Precautions
1) Keep it out of reach of children and guide and supervise children if they use it.
2) Avoid direct sunlight and keep the lid closed at room temperature. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other Information
- Questions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.LORD PROPOL WHITENING TOOTH
hydrogen peroxide, colloidal silicon dioxide, tocopherol acetate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82656-020 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Silicon Dioxide (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) Silicon Dioxide 7.0 g in 100 g Hydrogen Peroxide (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) Hydrogen Peroxide 2.14 g in 100 g .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE 0.2 g in 100 g Inactive Ingredients Ingredient Name Strength Sorbitol (UNII: 506T60A25R) Water (UNII: 059QF0KO0R) Xylitol (UNII: VCQ006KQ1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82656-020-02 1 in 1 CARTON 03/01/2022 1 NDC:82656-020-01 100 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 03/01/2022 Labeler - Red 99 (694767263) Registrant - Red 99 (694767263) Establishment Name Address ID/FEI Business Operations EQMAXON Corp. 557821534 manufacture(82656-020)
