NDC 21749-735 - PURELL Advanced Hand Sanitizer Refreshing Aloe Gel
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
- 21749-735
- Package NDCs from labels
- 21749-735-02, 21749-735-08, 21749-735-10, 21749-735-20
- Manufacturer
- GOJO Industries, LLC
- Effective date
- 2026-05-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PURELL Advanced Hand Sanitizer Refreshing Aloe Gel - GOJO Industries, LLC | GOJO Industries, LLC | 2026-05-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21749-735-02 | PURELL Advanced Hand Sanitizer Refreshing Aloe Gel | 60 mL in 1 BOTTLE | GEL | 60 | 1 | |
| 21749-735-08 | PURELL Advanced Hand Sanitizer Refreshing Aloe Gel | 236 mL in 1 BOTTLE | GEL | 236 | 1 | |
| 21749-735-10 | PURELL Advanced Hand Sanitizer Refreshing Aloe Gel | 295 mL in 1 BOTTLE | GEL | 295 | 1 | |
| 21749-735-20 | PURELL Advanced Hand Sanitizer Refreshing Aloe Gel | 591 mL in 1 BOTTLE | GEL | 591 | 1 |
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.