NDC 23243-2050 - Sacox 60
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
- 23243-2050
- Package NDCs from labels
- 23243-2050-5
- Manufacturer
- Huvepharma, Inc. | Huvepharma EOOD
- Effective date
- 2020-10-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sacox 60 - Huvepharma, Inc. | Huvepharma EOOD | Huvepharma, Inc. | Huvepharma EOOD | 2020-10-21 | OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| SALINOMYCIN | ACTIVE INGREDIENT | 62UXS86T64 | SACOX 60 (SALINOMYCIN) POWDER [HUVEPHARAMA, INC.] | 3 | |
| SALINOMYCIN | ACTIVE MOIETY | 62UXS86T64 | SACOX 60 (SALINOMYCIN) POWDER [HUVEPHARAMA, INC.] | 3 | |
| CALCIUM CARBONATE | INACTIVE INGREDIENT | H0G9379FGK | SACOX 60 (SALINOMYCIN) POWDER [HUVEPHARAMA, INC.] | 3 | |
| CALCIUM SILICATE | INACTIVE INGREDIENT | S4255P4G5M | SACOX 60 (SALINOMYCIN) POWDER [HUVEPHARAMA, INC.] | 3 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | SACOX 60 (SALINOMYCIN) POWDER [HUVEPHARAMA, INC.] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | SACOX 60 (SALINOMYCIN) POWDER [HUVEPHARAMA, INC.] | 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.