NDC 21749-300 - PURELL Alcohol Hand Sanitizing Wipes
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
- 21749-300
- Package NDCs from labels
- 21749-300-80, 21749-300-75
- Manufacturer
- GOJO Industries, Inc.
- Effective date
- 2025-11-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PURELL Alcohol Hand Sanitizing Wipes | GOJO Industries, Inc. | 2025-11-07 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 21749-300-75 | 2020-07-14 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-75 | 2020-07-14 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-80 | 2020-07-14 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-80 | 2020-07-14 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-75 | 2020-01-31 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-75 | 2020-01-31 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-80 | 2020-01-31 | PURELL Alcohol Hand Sanitizing Wipes |
| 21749-300-80 | 2020-01-31 | PURELL Alcohol Hand Sanitizing Wipes |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21749-300-75 | PURELL Alcohol Hand Sanitizing Wipes | 175 in 1 PACKAGE | CLOTH | 175 | 5 | |
| 21749-300-75 | PURELL Alcohol Hand Sanitizing Wipes | 479 mL in 1 PACKAGE | CLOTH | 479 | 5 | |
| 21749-300-80 | PURELL Alcohol Hand Sanitizing Wipes | 219 mL in 1 PACKAGE | CLOTH | 219 | 5 | |
| 21749-300-80 | PURELL Alcohol Hand Sanitizing Wipes | 80 in 1 PACKAGE | CLOTH | 80 | 5 |
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.