warnings
Warnings ● for external use only
Hydrocortisone
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Hydrocortisone
- Generic name
- HYDROCORTISONE
- Manufacturer
- TRIFECTA PHARMACEUTICALS USA LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1369e70f-7a61-7078-e063-6394a90a9a88
- SPL ID
- 1369e776-6fdf-6e18-e063-6394a90aee3b
- Version
- 1
- Effective date
- 2024-03-11
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:35:10
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M017 | openfda.application_number | |
| brand name | Hydrocortisone | openfda.brand_name | |
| generic name | HYDROCORTISONE | openfda.generic_name | |
| manufacturer name | TRIFECTA PHARMACEUTICALS USA LLC | openfda.manufacturer_name | |
| ndc | package | 69396-149-01 | openfda.package_ndc |
| ndc | product | 69396-149 | openfda.product_ndc |
| ndc11 | package | 69396014901 | derived:openfda.package_ndc |
| rxcui | 203105 | openfda.rxcui | |
| spl id | 1369e776-6fdf-6e18-e063-6394a90aee3b | id | |
| spl set id | 1369e70f-7a61-7078-e063-6394a90a9a88 | set_id | |
| unii | WI4X0X7BPJ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.