DOCTRUST DOUBLEX Tooth
- Product NDC
- 76670-0010
- 11-digit product format
- 766700010
- Labeler code
- 76670
- Product ID
- 76670-0010_2c47f6e9-359f-4f4e-e063-6394a90a6353
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- DOCSMEDI Co., Ltd.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-10-01
- Substance
- SODIUM FLUORIDE
- Active strength
- .22 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DOCTRUST DOUBLEX Tooth
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .22 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 245598 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76670-0010-1 | DOCTRUST DOUBLEX Tooth | 100 g in 1 TUBE | PASTE, DENTIFRICE | 100 | | 5 |
| 76670-0010-2 | DOCTRUST DOUBLEX Tooth | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76670-0010 | DOCTRUST DOUBLEX TOOTH (SODIUM FLUORIDE) PASTE, DENTIFRICE [DOCSMEDI CO., LTD.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250123_aaf08481-a2ff-48f6-8611-73a469efe1db.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76670-0010-1 | 76670001001 | 100 g in 1 TUBE | 100 g | | | | | Historical |
| 76670-0010-2 | 76670001002 | 1 TUBE in 1 CARTON (76670-0010-2) / 100 g in 1 TUBE (76670-0010-1) | 1 tube | 2021-10-01 | 0000-00-00 | No | No | Current |