NDC 21749-752-01 - PURELL Advanced Hygienic Hand Rub
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
- 21749-752
- Requested NDC
- 21749-752-01
- Package NDCs from labels
- 21749-752-01, 21749-752-02, 21749-752-04, 21749-752-12, 21749-752-16, 21749-752-97, 21749-752-80, 21749-752-10, 21749-752-89
- 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 Hygienic Hand Rub | GOJO Industries, Inc. | 2024-12-31 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21749-752-01 | PURELL Advanced Hygienic Hand Rub | 30 mL in 1 PACKAGE | GEL | 30 | 2 | |
| 21749-752-02 | PURELL Advanced Hygienic Hand Rub | 60 mL in 1 PACKAGE | GEL | 60 | 2 | |
| 21749-752-04 | PURELL Advanced Hygienic Hand Rub | 118 mL in 1 PACKAGE | GEL | 118 | 2 | |
| 21749-752-10 | PURELL Advanced Hygienic Hand Rub | 1000 mL in 1 PACKAGE | GEL | 1000 | 2 | |
| 21749-752-12 | PURELL Advanced Hygienic Hand Rub | 350 mL in 1 PACKAGE | GEL | 350 | 2 | |
| 21749-752-16 | PURELL Advanced Hygienic Hand Rub | 450 mL in 1 PACKAGE | GEL | 450 | 2 | |
| 21749-752-80 | PURELL Advanced Hygienic Hand Rub | 800 mL in 1 PACKAGE | GEL | 800 | 2 | |
| 21749-752-89 | PURELL Advanced Hygienic Hand Rub | 1200 mL in 1 PACKAGE | GEL | 1200 | 2 | |
| 21749-752-97 | PURELL Advanced Hygienic Hand Rub | 700 mL in 1 PACKAGE | GEL | 700 | 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.