Native
- Product NDC
- 37000-973
- 11-digit product format
- 370000973
- Labeler code
- 37000
- Product ID
- 37000-973_47e32c0d-afe6-af72-e063-6394a90af9cf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Procter & Gamble Manufacturing Company
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-01
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.4 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Native
- Brand name suffix
- Whitening
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.4 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 891775 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37000-973-41 | NativeWhitening | 116 g in 1 TUBE | PASTE, DENTIFRICE | 116 | | 7 |
| 37000-973-41 | NativeWhitening | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37000-973 | NATIVE WHITENING (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250115_a5248d35-f488-3457-e053-2995a90a411e.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 |
|---|
| 37000-973-41 | 37000097341 | 1 TUBE in 1 CARTON (37000-973-41) / 116 g in 1 TUBE | 1 tube | 2020-01-01 | 0000-00-00 | No | No | Current |