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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Teething | ARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEA | BioActive Nutritional, Inc. | f39c9feb-f567-43a2-a026-2a581aeeed9d | 2016-07-27 | Warnings | ETJ7Z6XBU4 |
| Antacid Relief | CALCIUM CARBONATE | Safeway | ead5101d-761a-4d1d-b14b-4dd548d2def6 | 2016-01-22 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.