warnings
Warnings for external use only
Hydrocortisone 1%
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 1%
- Generic name
- HYDROCORTISONE
- Manufacturer
- Trifecta Pharmaceuticals Usa Llc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c58904b5-ec72-4cf6-e053-2a95a90a2bfc
- SPL ID
- 299077a1-0e74-48ff-e063-6394a90a5246
- Version
- 4
- Effective date
- 2024-12-18
- Source export date
- 2026-11-06
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/f699a9578a0c5d6f5abd59491e85ce3c2c5e4567a51003fee350566c56ba5812/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:30:54
| 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 1% | openfda.brand_name | |
| generic name | HYDROCORTISONE | openfda.generic_name | |
| manufacturer name | Trifecta Pharmaceuticals Usa Llc | openfda.manufacturer_name | |
| ndc | package | 69396-081-01 | openfda.package_ndc |
| ndc | product | 69396-081 | openfda.product_ndc |
| ndc11 | package | 69396008101 | derived:openfda.package_ndc |
| rxcui | 106258 | openfda.rxcui | |
| spl id | 299077a1-0e74-48ff-e063-6394a90a5246 | id | |
| spl set id | c58904b5-ec72-4cf6-e053-2a95a90a2bfc | 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.