Firefly Bubble Gum Natural Fluoride
- Product NDC
- 66923-223
- 11-digit product format
- 669230223
- Labeler code
- 66923
- Product ID
- 66923-223_1749d24d-4e44-432d-9675-c1f83da01881
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium fluoride
- Dosage form
- POWDER, DENTIFRICE
- Route
- DENTAL
- Labeler
- Ranir LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-16
- Substance
- SODIUM FLUORIDE
- Active strength
- .24 g/100g
- 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
- Firefly Bubble Gum Natural Fluoride
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .24 g/100g |
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 |
|---|---|---|---|---|---|---|---|
| 66923-223-00 | 66923022300 | 119 g in 1 TUBE (66923-223-00) | 119 g | 2025-01-16 | No | No | Current |