NDC 76348-590-01 - Hemporrhoid
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
- 76348-590
- Requested NDC
- 76348-590-01
- Package NDCs from labels
- 76348-590-01, 76348-590-02
- Manufacturer
- Renu Laboratories, Inc.
- Effective date
- 2022-01-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HEMPORRHOID CREAM | Renu Laboratories, Inc. | 2022-01-14 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76348-590-02 | 2024-01-30 | C162847 | 48780-1 | 1030e365-05d4-111a-e063-dadaa90a10e2 | HEMPORRHOID CREAM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76348-590-01 | Hemporrhoid | 28 g in 1 TUBE | CREAM | 28 | 4 | |
| 76348-590-02 | Hemporrhoid | 1 in 1 BOX | CREAM | 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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.