Native
- Product NDC
- 37000-972
- 11-digit product format
- 370000972
- Labeler code
- 37000
- Product ID
- 37000-972_d60862ce-dc0f-6e2b-e053-2995a90ad495
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Procter & Gamble Manufacturing Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-01-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37000-972 | NATIVE CHARCOAL (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 6 | Legacy NDC | 20250110_a52460b4-1bb0-521a-e053-2995a90ad217.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37000-972-41 | 37000097241 | 1 TUBE in 1 CARTON (37000-972-41) > 116 g in 1 TUBE | 1 tube | 2020-01-01 | 0000-00-00 | No | No | Current |