FLUORIDEX
- Product NDC
- 59883-015
- 11-digit product format
- 598830015
- Labeler code
- 59883
- Product ID
- 59883-015_82f8ac58-f94c-255b-e053-2a91aa0aceb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- DEN-MAT HOLDINGS, LLC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-01-06
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 59883-015-04 | 59883001504 | 1 TUBE in 1 BOX (59883-015-04) > 112 g in 1 TUBE | 1 tube | 2017-01-06 | 0000-00-00 | No | No | Current |