CTx4 Gel 5000
- Product NDC
- 61578-206
- 11-digit product format
- 615780206
- Labeler code
- 61578
- Product ID
- 61578-206_deae5675-17c8-5972-e053-2a95a90adcc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- DENTAL ALLIANCE HOLDINGS LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-05-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 5000 ug/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61578-206-01 | 61578020601 | 56.699 g in 1 TUBE, WITH APPLICATOR (61578-206-01) | 56.699 g | 2022-05-10 | 0000-00-00 | No | No | Current |