NDC 21749-030 - PURELL Advanced Hand Sanitizer Foam
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
- 21749-030
- Package NDCs from labels
- 21749-030-89, 21749-030-97, 21749-030-53, 21749-030-17
- Manufacturer
- GOJO Industries, Inc.
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PURELL Advanced Hand Sanitizer Foam | GOJO Industries, Inc. | 2024-12-31 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21749-030-17 | PURELL Advanced Hand Sanitizer Foam | 515 mL in 1 PACKAGE | LIQUID | 515 | 6 | |
| 21749-030-53 | PURELL Advanced Hand Sanitizer Foam | 535 mL in 1 PACKAGE | LIQUID | 535 | 6 | |
| 21749-030-89 | PURELL Advanced Hand Sanitizer Foam | 1200 mL in 1 PACKAGE | LIQUID | 1200 | 6 | |
| 21749-030-97 | PURELL Advanced Hand Sanitizer Foam | 700 mL in 1 PACKAGE | LIQUID | 700 | 6 |
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.