NDC 75956-145-01 - Male Desensitizer Pleasure Balm
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
- 75956-145
- Requested NDC
- 75956-145-01
- Package NDCs from labels
- 75956-145-01, 75956-145-02
- Manufacturer
- Kama Sutra | Cosmetic Enterprise
- Effective date
- 2014-07-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Male Desensitizer Pleasure Balm - Kama Sutra | Cosmetic Enterprise | Kama Sutra | Cosmetic Enterprise | 2014-07-31 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75956-145-02 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-3516-60a7-e053-dbdaa90a05bd | Pleasure Balm |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75956-145-01 | Male DesensitizerPleasure Balm | 50 mL in 1 TUBE | GEL | 50 | 10 | |
| 75956-145-02 | Male DesensitizerPleasure Balm | 1 in 1 BOX | GEL | 1 | 10 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.