warnings
Warnings For external use only
ElixirCortiRelief
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
- ElixirCortiRelief
- Generic name
- HYDROCORTISONE
- Manufacturer
- ELIXIR HEALTHCARE USA, LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a6ca66f3-9759-4c98-a758-45700bc08352
- SPL ID
- 44f6ba8a-09f3-7425-e063-6294a90a740c
- Version
- 1
- Effective date
- 2025-12-02
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:57:13
| 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 | ElixirCortiRelief | openfda.brand_name | |
| generic name | HYDROCORTISONE | openfda.generic_name | |
| manufacturer name | ELIXIR HEALTHCARE USA, LLC. | openfda.manufacturer_name | |
| ndc | package | 84546-0005-1 | openfda.package_ndc |
| ndc | package | 84546-0005-2 | openfda.package_ndc |
| ndc | product | 84546-0005 | openfda.product_ndc |
| ndc11 | package | 84546000501 | derived:openfda.package_ndc |
| ndc11 | package | 84546000502 | derived:openfda.package_ndc |
| rxcui | 1043690 | openfda.rxcui | |
| spl id | 44f6ba8a-09f3-7425-e063-6294a90a740c | id | |
| spl set id | a6ca66f3-9759-4c98-a758-45700bc08352 | 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.