NDC 79332-005-01 - 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
- 79332-005
- Requested NDC
- 79332-005-01
- Package NDCs from labels
- 79332-005-01, 79332-005-08, 79332-005-04, 79332-005-02, 79332-005-80, 79332-005-16
- Manufacturer
- Zink Holdings LLC
- Effective date
- 2020-09-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hand Sanitizer - Zink Holdings LLC | Zink Holdings LLC | 2020-09-16 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79332-005-01 | Hand Sanitizer | 60 mL in 1 BOTTLE, PLASTIC | GEL | 60 | 2 | |
| 79332-005-02 | Hand Sanitizer | 1 in 1 BOX | GEL | 1 | 2 | |
| 79332-005-04 | Hand Sanitizer | 4 in 1 BOX | GEL | 4 | 2 | |
| 79332-005-08 | Hand Sanitizer | 8 in 1 BOX | GEL | 8 | 2 | |
| 79332-005-16 | Hand Sanitizer | 499 mL in 1 BOTTLE, PUMP | GEL | 499 | 2 | |
| 79332-005-80 | Hand Sanitizer | 236 mL in 1 BOTTLE, PUMP | GEL | 236 | 2 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.