Label: ORAL B NEUTRACARE MINT MENTHE- sodium fluoride solution
- NDC Code(s): 0273-0241-22
- Packager: YOUNG DENTAL MANUFACTURING CO 1, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 3, 2023
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INGREDIENTS AND APPEARANCE
ORAL B NEUTRACARE MINT MENTHE
sodium fluoride solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0273-0241 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.5 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) SPEARMINT OIL (UNII: C3M81465G5) SUCRALOSE (UNII: 96K6UQ3ZD4) PHOSPHORIC ACID (UNII: E4GA8884NN) SODIUM HYDROXIDE (UNII: 55X04QC32I) Product Characteristics Color Score Shape Size Flavor SPEARMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0273-0241-22 57 g in 1 TUBE; Type 0: Not a Combination Product 11/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/23/2014 Labeler - YOUNG DENTAL MANUFACTURING CO 1, LLC (006309355)