NEUTRAMAXX 5000
- Product NDC
- 63783-502
- 11-digit product format
- 637830502
- Labeler code
- 63783
- Product ID
- 63783-502_6e5e9034-b8fe-4c31-a51d-f1effafd8b15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- Massco Dental A Division of Dunagin Pharmaceuticals
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-08-01
- Marketing end
- 2023-12-31
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 g/112g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 63783-502 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 63783-502 | 63783-502-04 | D | Discontinued by firm | 2026-10-15 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63783-502-04 | 63783050204 | 112 g in 1 TUBE (63783-502-04) | 112 g | 2011-08-01 | 0000-00-00 | No | No | Current |