NDC 23851-057 - Happy Jack Ear Canker
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
- 23851-057
- Package NDCs from labels
- 23851-057-14
- Manufacturer
- Happy Jack Inc | Sigma-Aldrich Manufacturing LLC
- Effective date
- 2024-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Happy Jack Ear Canker - Happy Jack Inc | Sigma-Aldrich Manufacturing LLC | Happy Jack Inc | Sigma-Aldrich Manufacturing LLC | 2024-08-01 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 23851-057-14 | Happy Jack Ear Canker | 14 g in 1 BOTTLE, PLASTIC | POWDER | 14 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| iodoform | ACTIVE INGREDIENT | KXI2J76489 | HAPPY JACK EAR CANKER (ZINC OXIDE AND IODOFORM) POWDER [HAPPY JACK INC] | 1 | |
| zinc oxide | ACTIVE INGREDIENT | SOI2LOH54Z | HAPPY JACK EAR CANKER (ZINC OXIDE AND IODOFORM) POWDER [HAPPY JACK INC] | 1 | |
| iodoform | ACTIVE MOIETY | KXI2J76489 | HAPPY JACK EAR CANKER (ZINC OXIDE AND IODOFORM) POWDER [HAPPY JACK INC] | 1 | |
| zinc oxide | ACTIVE MOIETY | SOI2LOH54Z | HAPPY JACK EAR CANKER (ZINC OXIDE AND IODOFORM) POWDER [HAPPY JACK INC] | 1 | |
| calcium carbonate | INACTIVE INGREDIENT | H0G9379FGK | HAPPY JACK EAR CANKER (ZINC OXIDE AND IODOFORM) POWDER [HAPPY JACK INC] | 1 | |
| talc | INACTIVE INGREDIENT | 7SEV7J4R1U | HAPPY JACK EAR CANKER (ZINC OXIDE AND IODOFORM) POWDER [HAPPY JACK INC] | 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.