NDC 70233-005-01 - Male Genital Desensitizer Stud 100
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
- 70233-005
- Requested NDC
- 70233-005-01
- Package NDCs from labels
- 70233-005-01, 70233-005-02
- Manufacturer
- FLEET LABORATORIES LTD
- Effective date
- 2019-01-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Male Genital Desensitizer Stud 100 - FLEET LABORATORIES LTD | FLEET LABORATORIES LTD | 2019-01-08 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70233-005-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-0f2b-a910-e053-dadaa90a0b85 | Stud 100 Male Desensitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70233-005-01 | Male Genital DesensitizerStud 100 | 12.5 mL in 1 CAN | SPRAY, METERED | 12.5 | 4 | |
| 70233-005-02 | Male Genital DesensitizerStud 100 | 1 in 1 CARTON | SPRAY, METERED | 1 | 4 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Minnerva II | LIDOCAINE, EPINEPHRINE | SofTap Inc | ddd34237-7770-19b3-e053-2995a90af775 | 2022-05-05 | Warnings | 98PI200987 |
| lidocaine | LIDOCAINE | Proficient Rx LP | f9b290d2-0e24-4ca8-bca2-3016f5c404df | 2022-05-01 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Actavis Pharma, Inc. | 4d04052c-3e0a-469a-9265-99604f13e507 | 2022-04-30 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Proficient Rx LP | 2c396307-cf12-41d0-89e6-0f4ec74df55e | 2022-04-01 | Warnings, Adverse reactions | 98PI200987 |
| lidocaine | LIDOCAINE | Asclemed USA, Inc. | 6abf3773-0e60-48b1-9d5c-adc590363d13 | 2021-08-09 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Proficient Rx LP | f1007717-528a-42e2-94aa-db0edf3bb603 | 2021-01-01 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Asclemed USA, Inc. | c18f0c2b-cd05-4458-888f-47b4a1106937 | 2020-11-03 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Proficient Rx LP | cbf01b82-c43f-4bed-a1df-7569f4816c76 | 2019-11-01 | Warnings, Adverse reactions | 98PI200987 |
| 14ba62d0-4fca-401a-8717-0c79ce51c4d6 | db0e5117-88e9-42af-b09b-234e885f9a6e | 2019-01-08 | Warnings | 14ba62d0-4fca-401a-8717-0c79ce51c4d6 db0e5117-88e9-42af-b09b-234e885f9a6e | ||
| Cadira Compliant Blood Stat | LIDOCAINE / PRILOCAINE | Asclemed USA, Inc. | 79a31029-c221-4a4c-8dd9-bf78cbf2a16a | 2018-11-01 | Warnings, Adverse reactions | 98PI200987 |
| LIDO BDK | LIDOCAINE, PRILOCAINE | Asclemed USA, Inc. | 51fd0589-e551-4583-98e1-1e8db19d7e6d | 2018-11-01 | Warnings, Adverse reactions | 98PI200987 |
| Lidocaine | LIDOCAINE | Amneal Pharmaceuticals LLC | d1509740-f9f1-44e3-8fde-51d8683fcd87 | 2018-10-28 | Warnings, Adverse reactions | 98PI200987 |
| Soundbody | LIDOCAINE, MENTHOL | Kareway Product, Inc. | 6c83ec36-3e3d-07a9-e053-2a91aa0ac54c | 2018-05-18 | Warnings | 98PI200987 |
| Pure-Aid | LIDOCAINE, MENTHOL | Kareway Product, Inc. | 6679cada-f083-26e8-e053-2a91aa0adcc5 | 2018-03-02 | Warnings | 98PI200987 |
| Lidocaine Pain Relief Patch | LIDOCAINE AND MENTHOL, UNSPECIFIED FORM | Foshan Aqua Gel Biotech Co.,Ltd. | 3fe1a160-6508-62ea-e054-00144ff8d46c | 2017-11-06 | Warnings | 98PI200987 |
| Deeveeant Numb | LIDOCAINE | Valekista Limited | 2d7b39cc-4f1b-4414-b129-88c56e159aba | 2017-07-06 | Warnings | 98PI200987 |
| MediNumb | LIDOCAINE | Valekista Limited | 0e43648d-3dae-4faf-a6b4-d21c062e32e1 | 2017-07-06 | Warnings | 98PI200987 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.