Label: THE HUMBLE CO. KIT- sodium fluoride kit
- NDC Code(s): 72299-024-01, 72299-025-01
- Packager: The Humble Company North America Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 26, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Use
- Warning
-
Directions
Adults and children 2 years of age and 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 Instuct 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 a doctor. - Other information
- Inactive ingredients
- Questions?
- Package Labeling:Kit
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
THE HUMBLE CO. KIT
sodium fluoride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72299-024 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72299-024-01 1 in 1 KIT 02/01/2022 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 TUBE 6 g Part 1 of 1 HUMBLE CO FRESH MINT
sodium fluoride pasteProduct Information Item Code (Source) NDC:72299-025 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LAURYL SULFATE (UNII: 368GB5141J) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B) SACCHARIN SODIUM (UNII: SB8ZUX40TY) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72299-025-01 6 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 02/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 02/01/2022 Labeler - The Humble Company North America Inc (010966342)