NDC 21749-051 - GOJO Mild Antibacterial Foam Hand Sp
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
- 21749-051
- Package NDCs from labels
- 21749-051-53, 21749-051-97, 21749-051-89, 21749-051-90
- 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 |
|---|---|---|---|
| GOJO Mild Antibacterial Foam Hand Soap | GOJO Industries, Inc. | 2024-12-31 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21749-051-53 | GOJO Mild Antibacterial Foam Hand Sp | 535 mL in 1 PACKAGE | LIQUID | 535 | 5 | |
| 21749-051-89 | GOJO Mild Antibacterial Foam Hand Sp | 1200 mL in 1 PACKAGE | LIQUID | 1200 | 5 | |
| 21749-051-90 | GOJO Mild Antibacterial Foam Hand Sp | 1250 mL in 1 PACKAGE | LIQUID | 1250 | 5 | |
| 21749-051-97 | GOJO Mild Antibacterial Foam Hand Sp | 700 mL in 1 PACKAGE | LIQUID | 700 | 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.