Label: SODIUM FLUORIDE- clear mint, gel toothpaste gel
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NDC Code(s):
67777-180-01,
67777-180-02,
67777-180-03,
67777-180-04, view more67777-180-05, 67777-180-06, 67777-180-07, 67777-180-08, 67777-180-09, 67777-180-10, 67777-180-11
- Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 27, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use(s)
- Warnings
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Directions
• Adults and children 2 years of age and older: Brush teeth thoroughtly after meals or at least twice a day or use as directed by a dentist or physician.
• Children under 6 years: To minimize swallowing, use a pea sized amount and supervise child's brushing and rinsing until good habits are established.
• Children under 2 years: Ask a dentist or physician.
- Inactive Ingredients
- Other Information
- Questions?
- Label 5900
- Label 5901
- Label 5902
- Label 5903
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INGREDIENTS AND APPEARANCE
SODIUM FLUORIDE
clear mint, gel toothpaste gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-180 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 220 mg in 1 g Inactive Ingredients Ingredient Name Strength PEPPERMINT OIL (UNII: AV092KU4JH) SODIUM BENZOATE (UNII: OJ245FE5EU) POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4) HYDRATED SILICA (UNII: Y6O7T4G8P9) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) Product Characteristics Color Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-180-03 720 in 1 CASE 07/16/2024 1 NDC:67777-180-02 144 in 1 BOX 1 NDC:67777-180-01 17 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:67777-180-06 60 in 1 CASE 07/16/2024 2 NDC:67777-180-05 1 in 1 BOX 2 NDC:67777-180-04 130 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:67777-180-08 144 in 1 CASE 07/16/2024 3 NDC:67777-180-07 42.5 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:67777-180-11 720 in 1 CASE 07/16/2024 4 NDC:67777-180-10 144 in 1 BOX 4 NDC:67777-180-09 24 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 07/16/2024 Labeler - Dynarex Corporation (008124539)