OTC - ACTIVE INGREDIENT SECTION
Sodium monofluorophosphate 0.76% (0.13% w/v fluoride ion)
Sodium monofluorophosphate 0.76% (0.13% w/v fluoride ion)
Anticavity
Aids in teh prevention of dental cavities
Keep out of reach of children under 6 years of age. If you swallow more than a pea-sized dollop, get medical help or contact a poison control center right away.
Adults and children 6 years of age and older: our dentists recommend applying a pea-sized dollop of toothpaste on a soft-bristled toothbrush. Brush teeth thoroughly for 2 minutes twice a day, and not more than 3 times a day, or as recommended by your dentist or physician. Minimize swallowing. * Children under 6 years of age: consult a dentist or physician.
glycerin, water, calcium carbonate, hydrated silica, hydroxyapatite, xanthan gum, flavor, sodium lauroyl sarcosinate, benzyl alcohol, sodium bicarbonate
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 62721-5058 | 62721-5058-9 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CALCIUM CARBONATE | H0G9379FGK | IACT |
| HYDRATED SILICA | Y6O7T4G8P9 | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| SODIUM LAUROYL SARCOSINATE | 632GS99618 | IACT |
| TRIBASIC CALCIUM PHOSPHATE | 91D9GV0Z28 | IACT |
| SODIUM BICARBONATE | 8MDF5V39QO | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| SODIUM MONOFLUOROPHOSPHATE | C810JCZ56Q | ACTIM |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d4c376d5-4215-e1ac-e053-2995a90a518b | d36ffc66-5acc-df85-e053-2a95a90a26e8 | 2022-01-04 | Warnings | d4c376d5-4215-e1ac-e053-2995a90a518b d36ffc66-5acc-df85-e053-2a95a90a26e8 |
Adverse event summaries are temporarily unavailable. Other product information remains available.