GUM Cavity Prevention Fluoride Mint
- Product NDC
- 52376-086
- 11-digit product format
- 523760086
- Labeler code
- 52376
- Product ID
- 52376-086_93802930-37d3-4aca-9099-43d01a5951d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- Sunstar Americas, Inc.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-04-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52376-086-05 | 52376008605 | 24 g in 1 TUBE (52376-086-05) | 24 g | 2018-04-01 | 0000-00-00 | No | No | Current |