NDC 76348-595-01 - Numb Gel Anesthetic
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
- 76348-595
- Requested NDC
- 76348-595-01
- Package NDCs from labels
- 76348-595-01, 76348-595-02
- Manufacturer
- RENU LABORATORIES, INC.
- Effective date
- 2022-01-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| NUMB Gel Anesthetic | RENU LABORATORIES, INC. | 2022-01-17 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76348-595-02 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4573-111a-e063-dadaa90a10e2 | NUMB Gel Anesthetic |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76348-595-01 | Numb Gel Anesthetic | 28 g in 1 JAR | GEL | 28 | 3 | |
| 76348-595-02 | Numb Gel Anesthetic | 1 in 1 BOX | GEL | 1 | 3 |
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.