Freshmint-BD
- Product NDC
- 87846-009
- 11-digit product format
- 878460009
- Labeler code
- 87846
- Product ID
- 87846-009_5c35dd0f-3c35-1fe1-e063-6294a90a3bd8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Dabur India Limited
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-02
- Substance
- SODIUM FLUORIDE
- Active strength
- .24 g/1000g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Freshmint-BD
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .24 g/1000g |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 87846-009-20 | 87846000920 | 1 BOTTLE in 1 BOX (87846-009-20) / 113 g in 1 BOTTLE | 1 bottle | 2026-01-02 | No | No | Current |