NDC 27426-012-10 - Keratex KHW
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
- 27426-012
- Requested NDC
- 27426-012-10
- Package NDCs from labels
- 27426-012-10
- Manufacturer
- Penleigh Irving Ltd
- Effective date
- 2019-01-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Keratex KHW - Penleigh Irving Ltd | Penleigh Irving Ltd | 2019-01-02 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 27426-012-10 | KeratexKHW | 1 L in 1 BOTTLE, PLASTIC | LIQUID | 1 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZALKONIUM | ACTIVE INGREDIENT | 7N6JUD5X6Y | KERATEX KHW (BENZALKONIUM) LIQUID [PENLEIGH IRVING LTD] | 6 | |
| BENZALKONIUM | ACTIVE MOIETY | 7N6JUD5X6Y | KERATEX KHW (BENZALKONIUM) LIQUID [PENLEIGH IRVING LTD] | 6 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Walgreens Burn Gel Packettes | BURN GEL PACKETTES | Walgreens | 3fa09045-d4c0-8119-e063-6394a90ab6a0 | 2026-03-17 | Warnings | 7N6JUD5X6Y |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.