NDC 54340-171-07 - Dial Professional Gel Sanitizer
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
- 54340-171
- Requested NDC
- 54340-171-07
- Package NDCs from labels
- 54340-171-01, 54340-171-02, 54340-171-03, 54340-171-04, 54340-171-05, 54340-171-06, 54340-171-07, 54340-171-08, 54340-171-09, 54340-171-10
- Manufacturer
- Henkel Corporation
- Effective date
- 2026-02-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dial Professional Gel Sanitizer - Henkel Corporation | Henkel Corporation | 2026-02-27 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54340-171-01 | Dial Professional Gel Sanitizer | 1200 mL in 1 BOTTLE, DISPENSING | GEL | 1200 | 2 | |
| 54340-171-02 | Dial Professional Gel Sanitizer | 3 in 1 CARTON | GEL | 3 | 2 | |
| 54340-171-03 | Dial Professional Gel Sanitizer | 221 mL in 1 BOTTLE, PUMP | GEL | 221 | 2 | |
| 54340-171-04 | Dial Professional Gel Sanitizer | 12 in 1 CARTON | GEL | 12 | 2 | |
| 54340-171-05 | Dial Professional Gel Sanitizer | 443 mL in 1 POUCH | GEL | 443 | 2 | |
| 54340-171-06 | Dial Professional Gel Sanitizer | 6 in 1 CARTON | GEL | 6 | 2 | |
| 54340-171-07 | Dial Professional Gel Sanitizer | 1000 mL in 1 BOTTLE, DISPENSING | GEL | 1000 | 2 | |
| 54340-171-08 | Dial Professional Gel Sanitizer | 3 in 1 CARTON | GEL | 3 | 2 | |
| 54340-171-09 | Dial Professional Gel Sanitizer | 59 mL in 1 BOTTLE, DISPENSING | GEL | 59 | 2 | |
| 54340-171-10 | Dial Professional Gel Sanitizer | 144 in 1 CARTON | GEL | 144 | 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.