OTC - ACTIVE INGREDIENT SECTION
Stannous fluoride 0.454% w/w (0.15% w/v fluoride ion)
Stannous fluoride 0.454% w/w (0.15% w/v fluoride ion)
Anticavity, Antigingivitis, Antihypersensitivity
aids in teh prevention of dental cavities * helps interfere with the harmful effects of plaque associated with gingivitis * builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact
When using this product, if irritation occurs discontinue use.
Stop use and ask a dentist if:
the problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist * pain/sensitivity still persists after 4 weeks of use * gingivitis, bleeding, or redness persists for more than 2 weeks * you have painful or swollen gums, pus from the gum line, loose teeth, or increasing space between teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease.
Keep out of reach of children. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
adults and children 12 years of age and older: apply at least a 1-inch strip of the product onto a soft bristle toothbrush * brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Spit out after brushing. * children under 12 years of age: Consult a dentist or doctor.
products containing stannous fluoride may produce surface staining of the teeth. Adequate tooth brushing may prevent these stains which are not harmful or permanent and may be removed by your dentist. * this product is specifically formulated to help prevent staining. * store below 30°C (86°F)
glycerin, water, hydrated silica, pentasodium triphosphate, sodium lauryl sulfate, flavor, cellulose gum, titanium dioxide, cocamidopropyl betaine, sodium saccharin
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 416784 | stannous fluoride 0.454 % (fluoride ion 0.16 % ) Toothpaste | PSN | 7 |
| 416784 | stannous fluoride 0.00454 MG/MG Toothpaste | SCD | 7 |
| 416784 | stannous fluoride 0.454 % (fluoride ion 0.14 % ) Toothpaste | SY | 7 |
| 416784 | stannous fluoride 0.454 % (fluoride ion 0.15 % ) Toothpaste | SY | 7 |
| 416784 | stannous fluoride 0.454 % (fluoride ion 0.16 % ) Toothpaste | SY | 7 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69842-549-99 | CVS Complete Protection | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | 7 | |
| 69842-549-99 | CVS Complete Protection | 96.4 g in 1 TUBE | PASTE, DENTIFRICE | 96.4 | 7 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 69842-549 | 69842-549-99 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| STANNOUS FLUORIDE | 3FTR44B32Q | ACTIM |
| WATER | 059QF0KO0R | IACT |
| SACCHARIN SODIUM | SB8ZUX40TY | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | IACT |
| HYDRATED SILICA | Y6O7T4G8P9 | IACT |
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| SODIUM LAURYL SULFATE | 368GB5141J | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| SODIUM TRIPOLYPHOSPHATE ANHYDROUS | 9SW4PFD2FZ | IACT |
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 6 | 2025-11-13 | monthly-update | 2026-06-03 17:39:57 |
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 |
|---|---|---|---|---|---|---|
| CVS Complete Protection | STANNOUS FLOURIDE | CVS | b681b5e4-a0e1-8d0f-e053-2a95a90aa672 | 2026-01-06 | Warnings | 69842-549-99 69842-549 69842054999 47b7b772-763d-836e-e063-6394a90ab371 b681b5e4-a0e1-8d0f-e053-2a95a90aa672 |
Adverse event summaries are temporarily unavailable. Other product information remains available.