Label: BIO SPECTRA ATTITUDE- sodium fluoride gel, dentifrice
- NDC Code(s): 61649-723-01
- Packager: 9055-7588 Québec Inc. DBA Attitude
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 2, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
Do not swallow. Should be used as part of an oral health program that includes regular flossing and dental check-ups. Brush teeth thoroughly for at least 1 minute twice a day, preferably after each meal, or as directed by a dentist. Children under 6 years of age should use only a pea-sized amount and be supervised to brush properly and to not swallow. Consult a dentist or health care professional before using with children under 2 years of age. Store at room temperature (15-30 °C).
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Inactive ingredients
Aqua / Water / Eau, Sorbitol, Glycerin, Hydrated Silica, Sodium Lauryl Sulfate, Xanthan Gum, Citric Acid, Rebaudioside A, Sodium Benzoate, Potassium Sorbate, Carica Papaya (Papaya) Leaf Extract, Camellia Sinensis (Tea) Leaf Extract, Alpha-Ionone*, Butyl Isovalerate*, Caprylic/Capric Triglyceride*, Ethyl Butyrate*, Gamma-Decalactone*, *flavour (Aroma).
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- PRINCIPAL DISPLAY PANEL - 120 g Tube Label
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INGREDIENTS AND APPEARANCE
BIO SPECTRA ATTITUDE
sodium fluoride gel, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61649-723 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 0.243 g in 100 g Inactive Ingredients Ingredient Name Strength SORBITOL (UNII: 506T60A25R) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM LAURYL SULFATE (UNII: 368GB5141J) XANTHAN GUM (UNII: TTV12P4NEE) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) REBAUDIOSIDE A (UNII: B3FUD0528F) SODIUM BENZOATE (UNII: OJ245FE5EU) CARICA PAPAYA LEAF (UNII: 66J7636Z2I) GREEN TEA LEAF (UNII: W2ZU1RY8B0) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ETHYL BUTYRATE (UNII: UFD2LZ005D) BUTYL ISOVALERATE (UNII: 4UX6V9QM2J) .GAMMA.-DECALACTONE (UNII: 7HLS05KP9O) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) .ALPHA.-IONONE (UNII: I9V075M61R) Product Characteristics Color white (Opaque) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61649-723-01 120 g in 1 TUBE; Type 0: Not a Combination Product 05/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 05/15/2021 Labeler - 9055-7588 Québec Inc. DBA Attitude (201137051) Establishment Name Address ID/FEI Business Operations 9055-7588 Québec Inc. DBA Attitude 204307099 manufacture(61649-723) , label(61649-723) , pack(61649-723) , analysis(61649-723)