OTC - ACTIVE INGREDIENT SECTION
Potassium nitrate 5%....................................................Antihypersensitivity
Sodium fluoride 0.24% (0.15% w/v fluoride ion)............Anticavity
Potassium nitrate 5%....................................................Antihypersensitivity
Sodium fluoride 0.24% (0.15% w/v fluoride ion)............Anticavity
water, hydrated silica, sorbitol, glycerin, cocamidopropyl betaine, PEG-12, titanium dioxide, cellulose gum, flavor, sodium benzoate, sodium saccharin, red 40
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/esnsitivty still persists after 4 weeks of use.
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 one minute twice a day (morning and evening), and nore 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.
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 one minute twice a day (morning and evening), and nore 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.
If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 83324-291 | 83324-291-34 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| POTASSIUM NITRATE | RU45X2JN0Z | ACTIB |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM | K679OBS311 | IACT |
| HYDRATED SILICA | Y6O7T4G8P9 | IACT |
| SODIUM FLUORIDE | 8ZYQ1474W7 | ACTIM |
| SACCHARIN SODIUM | SB8ZUX40TY | IACT |
| PEG-12 | NL4J9F21N9 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| SORBITOL | 506T60A25R | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| WATER | 059QF0KO0R | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
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 |
|---|---|---|---|---|---|---|
| Quality Choice Natural White | FLUORIDE | CHAIN DRUG MARKETING ASSOCIATION INC | 561a75c2-a40c-ba7c-e063-6294a90aa119 | 2026-07-08 | Warnings | 83324-291-34 83324-291 83324029134 561a75c2-a40d-ba7c-e063-6294a90aa119 561a75c2-a40c-ba7c-e063-6294a90aa119 |
Adverse event summaries are temporarily unavailable. Other product information remains available.