NDC 52261-0801-01 - Keeps Climax Delay
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
- 52261-0801
- Requested NDC
- 52261-0801-01
- Package NDCs from labels
- 52261-0801-1, 52261-0801-01
- Manufacturer
- Cosco International, Inc.
- Effective date
- 2026-03-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Keeps Climax Delay Spray | Cosco International, Inc. | 2026-03-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52261-0801-1 | Keeps Climax Delay | 1 in 1 CARTON | LIQUID | 1 | 2 | |
| 52261-0801-1 | Keeps Climax Delay | 0.00052 kg in 1 BOTTLE, SPRAY | LIQUID | 0.00052 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52261-0801 | KEEPS CLIMAX DELAY (LIDOCAINE HYDROCHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.] | 1 | Current NDC, 2 package rows | 20240619_3bfd3173-2dac-40a9-aec3-982b1d47d8fa.zip |
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.