OTC - ACTIVE INGREDIENT SECTION
Active ingredient : Sodium fluoride
Active ingredient : Sodium fluoride
Preservatives-Sodium Benzoate
Other additives-L-Menthol, Sophora Angustifolia Root Extract, Glycyrrhiza Inflata Root Extract, Glycerin, Camellia Sinensis Catechins, Saccharin Sodium Hydrate, Sodium Citrate Hydrate, Citric Acid Hydrate, Xylitol, DI-Water, Caramel Colorant, Red Ginseng Extract, Polyoxyl 40 Hydrogenated Castor Oil
prevent cavities, and remove bad breath
Keep out of reach of children
● Administration and doses : Once a day (mainly before bed), use it after brushing thoroughly. 6 years old to adults:10ml into your mouth, mix well for 1 minute, then spit. Be careful not to eat or drink food for 30 minutes after use to obtain sufficient effect.
● Caution : 1) The fluoride content of this product is 90.5ppm. 2) Do not use this product - Anyone who is hypersensitive to this product. 3) Other Precautions when using this product-Do not swallow. Do not use for children under 6 years old unless instructed by a dentist. Keep out of reach of children. If they drink lots of medicine, feed large amounts of milk and follow doctor's instructions. 4) Storage precautions and other precautions when using this product-Keep out of the reach of children. Avoid direct sunlight. To shade the light, store in a cool place. To prevent misuse and preserve quality, do not change the container.
For dental use only
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69255-200-01 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-426c-a910-e053-dadaa90a0b85 | 7f10d5a6-2d5b-7ce2-e053-2991aa0ab425 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69255-200-01 | Dr. 9020 Dental Clinic | 260 mL in 1 BOTTLE | LIQUID | 260 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 69255-200 | 69255-200-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| XYLITOL | VCQ006KQ1E | IACT |
| LEVOMENTHOL | BZ1R15MTK7 | IACT |
| SODIUM FLUORIDE | 8ZYQ1474W7 | 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 |
|---|---|---|---|---|---|---|
| 7f10d5a6-2d5c-7ce2-e053-2991aa0ab425 | 7f10d5a6-2d5b-7ce2-e053-2991aa0ab425 | 2019-01-09 | Warnings | 7f10d5a6-2d5c-7ce2-e053-2991aa0ab425 7f10d5a6-2d5b-7ce2-e053-2991aa0ab425 |
Adverse event summaries are temporarily unavailable. Other product information remains available.