NDC 70233-004-01 - Premjact Male Desensitizer Pound International
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70233-004
- Requested NDC
- 70233-004-01
- Package NDCs from labels
- 70233-004-01, 70233-004-02
- Manufacturer
- FLEET LABORATORIES LTD
- Effective date
- 2017-01-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Premjact Male Desensitizer Pound International - FLEET LABORATORIES LTD | FLEET LABORATORIES LTD | 2017-01-03 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70233-004-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-04aa-f424-e053-dadaa90a57ce | Premjact Male Genital Desensitizer Spray |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70233-004-01 | Premjact Male DesensitizerPound International | 12 mL in 1 CAN | SPRAY, METERED | 12 | 2 | |
| 70233-004-02 | Premjact Male DesensitizerPound International | 1 in 1 CARTON | SPRAY, METERED | 1 | 2 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.