NDC 24730-503 - ProPet
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
- 24730-503
- Package NDCs from labels
- 24730-503-04
- Manufacturer
- United Pet Group | JUNGLE LABORATORIES CORPORATION
- Effective date
- 2010-01-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ProPet - United Pet Group | JUNGLE LABORATORIES CORPORATION | United Pet Group | JUNGLE LABORATORIES CORPORATION | 2010-01-26 | OTC ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Hydrocortisone | ACTIVE INGREDIENT | WI4X0X7BPJ | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| Hydrocortisone | ACTIVE MOIETY | WI4X0X7BPJ | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| ALOE VERA LEAF | INACTIVE INGREDIENT | ZY81Z83H0X | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| DIAZOLIDINYL UREA | INACTIVE INGREDIENT | H5RIZ3MPW4 | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| METHYLPARABEN | INACTIVE INGREDIENT | A2I8C7HI9T | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| PROPYLPARABEN | INACTIVE INGREDIENT | Z8IX2SC1OH | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | PROPET (ITCH RELIEF HYDROCORTISONE) SPRAY [UNITED PET GROUP] | 3 |
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.