Label: WHITE GLO PROFESSIONAL CHOICE TWIN PACK- sodium fluoride kit
- NDC Code(s): 73656-024-00, 73656-025-00
- Packager: WHITE GLO USA INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 18, 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. Children under 2 years of age: Consult a dentist or doctor.
- Other information
- Inactive ingredients
- Questions or comments
- Package Labeling:
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INGREDIENTS AND APPEARANCE
WHITE GLO PROFESSIONAL CHOICE TWIN PACK
sodium fluoride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73656-024 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73656-024-00 1 in 1 BOX 10/19/2023 1 1 in 1 KIT Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 TUBE 300 g Part 1 of 1 WHITE GLO PROFESSIONAL CHOICE
sodium fluoride paste, dentifriceProduct Information Item Code (Source) NDC:73656-025 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1 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) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM SILICATE (UNII: IJF18F77L3) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73656-025-00 150 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 M021 10/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 10/19/2023 Labeler - WHITE GLO USA INC (117345666)