DOCTRUST DOUBLEX Tooth
- Product NDC
- 73242-1122
- 11-digit product format
- 732421122
- Labeler code
- 73242
- Product ID
- 73242-1122_44765e86-2eb3-6381-e063-6394a90a761f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- DONG IL PHARMS 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 |
|---|
| 73242-1122-1 | DOCTRUST DOUBLEX Tooth | 100 g in 1 TUBE | PASTE, DENTIFRICE | 100 | | 1 |
| 73242-1122-2 | DOCTRUST DOUBLEX Tooth | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73242-1122-1 | 73242112201 | 100 g in 1 TUBE | 100 g | | | | Historical |
| 73242-1122-2 | 73242112202 | 1 TUBE in 1 CARTON (73242-1122-2) / 100 g in 1 TUBE (73242-1122-1) | 1 tube | 2021-10-01 | No | No | Current |