Meridian Anticavity
- Product NDC
- 53247-145
- 11-digit product format
- 532470145
- Labeler code
- 53247
- Product ID
- 53247-145_8fe7876a-1dca-4c7e-afda-2482a5d550a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Bob Barker Company Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-14
- Substance
- SODIUM FLUORIDE
- Active strength
- 2.2 mg/g
- 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
- Meridian Anticavity
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | 2.2 mg/g |
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 |
|---|---|---|---|---|---|---|---|
| 53247-145-01 | 53247014501 | 4.3 g in 1 PACKET (53247-145-01) | 4.3 g | 2026-09-14 | No | No | Current |
| 53247-145-02 | 53247014502 | 17 g in 1 TUBE (53247-145-02) | 17 g | 2026-09-14 | No | No | Current |
| 53247-145-03 | 53247014503 | 24 g in 1 TUBE (53247-145-03) | 24 g | 2026-09-14 | No | No | Current |
| 53247-145-04 | 53247014504 | 43 g in 1 TUBE (53247-145-04) | 43 g | 2026-09-14 | No | No | Current |
| 53247-145-05 | 53247014505 | 130 g in 1 TUBE (53247-145-05) | 130 g | 2026-09-14 | No | No | Current |