OTC - ACTIVE INGREDIENT SECTION
Silicon Dioxide (Dental Type Silica), Sodium Pyrophosphate (Tetrasodium Pyrophosphate)
Silicon Dioxide (Dental Type Silica), Sodium Pyrophosphate (Tetrasodium Pyrophosphate)
D-Sorbitol Solution, Concentrated Glycerin, Xanthangum, Sodium Cocoyl Glutamate, Ascorbic Acid, Hydroxyapatite, Xylitol, Sodium Chloride, Green Tea Extract, Eucalyptus Extract, Matricaria Extract, Aloe Extract, Sage Extract, Grapefruit Seed Extract, Natural Strawberry Flavor, Water
ANTI-CAVITY
Keep out of reach of children
Put an appropriate amount on a toothbrush and brush teeth.
Storage method
1. Keep it at room temperature in a classified container.
2. Cover and store at room temperature.
3. Store in a not moisture and cool place.
4. Air may come out during use of this product, but there is no problem with its weight.
Usage Precautions
1. Be careful not to swallow. Rinse mouth thoroughly after use
2. If the use of toothpaste causes abnormalities such as gums or mouth injury, discontinue use and consult a doctor or dentist.
3. For children under 6 years of age, use a small amount of toothpaste as small as pea per use, and use under the guidance of a guardian to avoid sucking or swallowing.
4. If a child under 6 years old swallows large amount, consult with a doctor or dentist immediately.
5. Keep out of the reach of children under 6 years of age.
For dental use only
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76884-0003-1 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-66f6-d83d-e063-dadaa90ab31f | b663cd76-97b7-28b2-e053-2a95a90af422 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76884-0003-1 | Dr. DADDYS Tooth | 60 g in 1 TUBE | PASTE, DENTIFRICE | 60 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 76884-0003 | DR. DADDYS TOOTH (DENTAL TYPE SILICA, TETRASODIUM PYROPHOSPHATE) PASTE, DENTIFRICE [TB HEALTHCARE CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20201217_b663cd76-97b7-28b2-e053-2a95a90af422.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 76884-0003 | 76884-0003-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| XYLITOL | VCQ006KQ1E | IACT |
| WATER | 059QF0KO0R | IACT |
| SORBITOL | 506T60A25R | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| SODIUM PYROPHOSPHATE | O352864B8Z | ACTIB |
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 |
|---|---|---|---|---|---|---|
| b663cd60-75dd-6bc5-e053-2995a90a9477 | b663cd76-97b7-28b2-e053-2a95a90af422 | 2020-12-13 | Warnings | b663cd60-75dd-6bc5-e053-2995a90a9477 b663cd76-97b7-28b2-e053-2a95a90af422 |
Adverse event summaries are temporarily unavailable. Other product information remains available.