NDC 0049-0670 - Terra-Cortril
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
- 0049-0670
- Package NDCs from labels
- 0049-0670-48
- Manufacturer
- Roerig
- Effective date
- 2006-04-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Terra-Cortril - Roerig | Roerig | 2006-04-07 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| hydrocortisone acetate | ACTIVE INGREDIENT | 3X7931PO74 | TERRA-CORTRIL (OXYTETRACYCLINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE) SUSPENSION [ROERIG] | 1 | |
| oxytetracycline hydrochloride | ACTIVE INGREDIENT | 4U7K4N52ZM | TERRA-CORTRIL (OXYTETRACYCLINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE) SUSPENSION [ROERIG] | 1 | |
| hydrocortisone | ACTIVE MOIETY | WI4X0X7BPJ | TERRA-CORTRIL (OXYTETRACYCLINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE) SUSPENSION [ROERIG] | 1 | |
| oxytetracycline | ACTIVE MOIETY | X20I9EN955 | TERRA-CORTRIL (OXYTETRACYCLINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE) SUSPENSION [ROERIG] | 1 | |
| aluminum tristearate | INACTIVE INGREDIENT | U6XF9NP8HM | TERRA-CORTRIL (OXYTETRACYCLINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE) SUSPENSION [ROERIG] | 1 | |
| mineral oil | INACTIVE INGREDIENT | TERRA-CORTRIL (OXYTETRACYCLINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE) SUSPENSION [ROERIG] | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 7BFF901E-0496-4818-813A-108B762B83A8 | 7BFF901E-0496-4818-813A-108B762B83A8 | 2006-04-07 | Warnings, Adverse reactions | 7BFF901E-0496-4818-813A-108B762B83A8 7BFF901E-0496-4818-813A-108B762B83A8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.