NDC 76913-615-01 - Hand Sanitizer
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
- 76913-615
- Requested NDC
- 76913-615-01
- Package NDCs from labels
- 76913-615-01, 76913-615-02, 76913-615-03, 76913-615-04
- Manufacturer
- Nova Pressroom Products LLC
- Effective date
- 2020-10-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hand Sanitizer - Nova Pressroom Products LLC | Nova Pressroom Products LLC | 2020-10-22 | HUMAN OTC DRUG LABEL |
| Hand Sanitizer - Nova Pressroom Products LLC | Nova Pressroom Products LLC | 2020-04-30 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Indexing SPL | Related label |
|---|---|---|---|
| 76913-615-02 | 2025-11-12 | d6a99b39-fe16-a426-e053-dadaa90af4c2 | a4606fd3-3ca9-3e50-e053-2995a90a8c64 |
| 76913-615-04 | 2025-11-12 | d6a99b39-7039-a426-e053-dadaa90af4c2 | a483ea3a-0794-6016-e053-2a95a90a70ca |
| 76913-615-02 | 2022-01-28 | d6a99b39-fe16-a426-e053-dadaa90af4c2 | a4606fd3-3ca9-3e50-e053-2995a90a8c64 |
| 76913-615-04 | 2022-01-28 | d6a99b39-7039-a426-e053-dadaa90af4c2 | a483ea3a-0794-6016-e053-2a95a90a70ca |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 76913-615 | HAND SANITIZER (ALCOHOL) OINTMENT [NOVA PRESSROOM PRODUCTS LLC] | 2 | Legacy NDC | 20201023_a4606fd3-3ca9-3e50-e053-2995a90a8c64.zip |
| 76913-615 | HAND SANITIZER (ALCOHOL) OINTMENT [NOVA PRESSROOM PRODUCTS LLC] | 1 | Legacy NDC | 20200501_a483ea3a-0794-6016-e053-2a95a90a70ca.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.