Label: WHITE GLO MICELLAR- sodium monofluorophosphate kit
- NDC Code(s): 73656-003-00, 73656-004-00
- Packager: WHITE GLO USA INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Use
- Warnings
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Directions
Adults and children 2 years of age & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children under 6 years of age: Instruct in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Consult a dentist or doctor. Children under 2 years of age:
- Other information
- Inactive ingredients
- Questions or comments
- Package Labeling:
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INGREDIENTS AND APPEARANCE
WHITE GLO MICELLAR
sodium monofluorophosphate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73656-003 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73656-003-00 1 in 1 KIT 02/15/2020 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 TUBE 150 g Part 1 of 1 WHITE GLO MICELLAR
sodium monofluorophosphate paste, dentifriceProduct Information Item Code (Source) NDC:73656-004 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 7.6 mg in 1 g Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE (UNII: H0G9379FGK) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM LAURYL SULFATE (UNII: 368GB5141J) METHYL SALICYLATE (UNII: LAV5U5022Y) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM SILICATE (UNII: IJF18F77L3) SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73656-004-00 150 g in 1 TUBE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 02/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 02/15/2020 Labeler - WHITE GLO USA INC (117345666)