Crest 3D White
- Product NDC
- 69423-943
- 11-digit product format
- 694230943
- Labeler code
- 69423
- Product ID
- 69423-943_f1ed8737-025a-59b9-e053-2a95a90a1177
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-01-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 | 69423-943 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 69423-943 | 69423-943-02 | D | Discontinued by firm | 2026-10-15 | |
| excluded package | package | 69423-943 | 69423-943-04 | D | Discontinued by firm | 2026-10-15 | |
| excluded package | package | 69423-943 | 69423-943-37 | D | Discontinued by firm | 2026-10-15 | |
| excluded package | package | 69423-943 | 69423-943-40 | D | Discontinued by firm | 2026-10-15 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Dataset | Scope | Package NDC |
|---|---|---|
| excluded product | product | |
| excluded package | package | 69423-943-04 |
| excluded package | package | 69423-943-40 |
| excluded package | package | 69423-943-37 |
| excluded package | package | 69423-943-02 |
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 |
|---|---|---|---|---|---|---|---|---|
| 69423-943-02 | 69423094302 | 2 TUBE in 1 CARTON (69423-943-02) > 104 g in 1 TUBE | 2 tube | 2021-08-01 | 0000-00-00 | No | No | Current |
| 69423-943-04 | 69423094304 | 4 CARTON in 1 CELLO PACK (69423-943-04) > 1 TUBE in 1 CARTON > 113 g in 1 TUBE | 4 carton | 2021-01-01 | 0000-00-00 | No | No | Current |
| 69423-943-37 | 69423094337 | 1 TUBE in 1 CARTON (69423-943-37) > 104 g in 1 TUBE | 1 tube | 2021-08-01 | 0000-00-00 | No | No | Current |
| 69423-943-40 | 69423094340 | 1 TUBE in 1 CARTON (69423-943-40) > 113 g in 1 TUBE | 1 tube | 2021-01-01 | 0000-00-00 | No | No | Current |