Colgate Cavity Protection Fresh Mint
- Product NDC
- 35000-914
- 11-digit product format
- 350000914
- Labeler code
- 35000
- Product ID
- 35000-914_4dd27637-354c-4f8f-b622-b4f0bf0d0f62
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate-Palmolive Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-08-05
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | 35000-914 | D | Discontinued by firm | 2026-10-16 | ||
| excluded package | package | 35000-914 | 35000-914-69 | D | Discontinued by firm | 2026-10-16 |
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 |
|---|---|---|---|---|---|---|---|---|
| 35000-914-69 | 35000091469 | 113 g in 1 TUBE (35000-914-69) | 113 g | 2019-08-05 | 0000-00-00 | No | No | Current |