Label: OPALESCENCE SENSITIVITY RELIEF WHITENING- potassium nitrate and sodium fluoride gel, dentifrice
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NDC Code(s):
51206-308-01,
51206-308-02,
51206-308-03,
51206-308-04, view more51206-308-05, 51206-308-06
- Packager: Ultradent Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 22, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
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Directions
- Adults and children 12 years of age and older: Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth.
- Children under 12 years of age: Consult a dentist or doctor.
- Other Information
- Inactive Ingredients
- Questions or comments
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 133 g Tube Carton
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INGREDIENTS AND APPEARANCE
OPALESCENCE SENSITIVITY RELIEF WHITENING
potassium nitrate and sodium fluoride gel, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51206-308 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE 50 mg in 1 g SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.1 mg in 1 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) SODIUM HYDROXIDE (UNII: 55X04QC32I) XYLITOL (UNII: VCQ006KQ1E) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) METHYL SALICYLATE (UNII: LAV5U5022Y) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Product Characteristics Color green Score Shape Size Flavor MINT (Cool Mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51206-308-01 1 in 1 CARTON 11/30/2015 1 28.35 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:51206-308-05 24 in 1 PACKAGE, COMBINATION 11/30/2015 2 1 in 1 CARTON 2 28.35 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:51206-308-02 1 in 1 CARTON 11/30/2015 3 133 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:51206-308-03 3 in 1 PACKAGE, COMBINATION 11/30/2015 4 1 in 1 CARTON 4 133 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:51206-308-04 12 in 1 PACKAGE, COMBINATION 11/30/2015 5 1 in 1 CARTON 5 133 g in 1 TUBE; Type 0: Not a Combination Product 6 NDC:51206-308-06 6 in 1 PACKAGE, COMBINATION 11/30/2015 6 1 in 1 CARTON 6 133 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 OTC Monograph Drug M022 11/30/2015 Labeler - Ultradent Products, Inc. (013369913) Establishment Name Address ID/FEI Business Operations Ultradent Products, Inc. 013369913 manufacture(51206-308) , analysis(51206-308) , label(51206-308) , pack(51206-308)