Dr. Jen SuperPaste Nano-Hydroxyapatite
- Product NDC
- 84181-735
- 11-digit product format
- 841810735
- Labeler code
- 84181
- Product ID
- 84181-735_dd378bbc-c051-4dcc-aa69-859b99e29cd3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- Dr Jen Natural, LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-21
- Substance
- SODIUM FLUORIDE
- Active strength
- .22 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr. Jen SuperPaste Nano-Hydroxyapatite
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .22 g/100mL |
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 |
|---|
| 84181-735-07 | Dr. Jen SuperPaste Nano-Hydroxyapatite | 1 in 1 BOX | PASTE, DENTIFRICE | 1 | | 2 |
| 84181-735-07 | Dr. Jen SuperPaste Nano-Hydroxyapatite | 100 mL in 1 TUBE | PASTE, DENTIFRICE | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84181-735 | DR. JEN SUPERPASTE NANO-HYDROXYAPATITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [DR JEN NATURAL, LLC] | 1 | Current NDC, 2 package rows | 20240329_8b28b857-9162-4065-b0a0-571efffe9787.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84181-735-07 | 84181073507 | 1 TUBE in 1 BOX (84181-735-07) / 100 mL in 1 TUBE | 1 tube | 2024-03-21 | No | No | Historical |