NDC 79481-0135-01 - Meijer Antibacterial Amber Hand
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
- 79481-0135
- Requested NDC
- 79481-0135-01
- Package NDCs from labels
- 79481-0135-1, 79481-0135-01
- Manufacturer
- Meijer, Inc.
- Effective date
- 2026-07-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Meijer ® Antibacterial Hand Soap | Meijer, Inc. | 2026-07-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0135-1 | Meijer Antibacterial White Tea and Berry Hand | 221 mL in 1 BOTTLE, PUMP | SOAP | 221 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0135 | MEIJER ANTIBACTERIAL SPRING RAIN HAND (BENZALKONIUM CHLORIDE) SOAP MEIJER ANTIBACTERIAL AMBER HAND (BENZALKONIUM CHLORIDE) SOAP MEIJER ANTIBACTERIAL WHITE TEA AND BERRY HAND (BENZALKONIUM CHLORIDE) SOAP [MEIJER, INC.] | 1 | Current NDC, 1 package rows | 20250529_35bbdd67-6d15-26b6-e063-6394a90a3f96.zip |
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.