Darby
- Product NDC
- 66467-2130
- 11-digit product format
- 664672130
- Labeler code
- 66467
- Product ID
- 66467-2130_7ddf03b2-5368-4001-e053-2991aa0ae027
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- Darby Dental Supply, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-11-09
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 66467-2130 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 66467-2130 | 66467-2130-1 | D | Discontinued by firm | 2026-07-31 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| sodium fluoride | ACTIVE INGREDIENT | 8ZYQ1474W7 | DARBY (SODIUM FLUORIDE) GEL [DARBY DENTAL SUPPLY CO INC] | 1 | |
| fluoride ion | ACTIVE MOIETY | Q80VPU408O | DARBY (SODIUM FLUORIDE) GEL [DARBY DENTAL SUPPLY CO INC] | 1 |