NDC 54340-016-01 - Dial Foaming Antibacterial and Moisturizing Hand Wash Spring Water
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
- 54340-016
- Requested NDC
- 54340-016-01
- Package NDCs from labels
- 54340-016-01, 54340-016-02, 54340-016-03
- Manufacturer
- Henkel Corporation
- Effective date
- 2025-12-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Benzalkonium Chloride - Henkel Corporation | Henkel Corporation | 2025-12-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54340-016-01 | Dial Foaming Antibacterial and Moisturizing Hand Wash Spring Water | 221 mL in 1 BOTTLE, DISPENSING | SOLUTION | 221 | 1 | |
| 54340-016-02 | Dial Foaming Antibacterial and Moisturizing Hand Wash Spring Water | 4 in 1 PACKAGE | SOLUTION | 4 | 1 | |
| 54340-016-03 | Dial Foaming Antibacterial and Moisturizing Hand Wash Spring Water | 198 in 1 CARTON | SOLUTION | 198 | 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.