warnings
Warnings for external use only
Thera Plus
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
- Thera Plus
- Generic name
- HYDROCORTISONE
- Manufacturer
- Zhejiang Jingwei Pharmaceutical Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- bcc99e5a-2403-46da-9c9d-8411fa4104e0
- SPL ID
- 08849eb4-ae6b-8151-e063-6394a90a5a7e
- Version
- 7
- Effective date
- 2023-10-25
- Source export date
- 2026-10-30
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:28:30
| 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 | Thera Plus | openfda.brand_name | |
| generic name | HYDROCORTISONE | openfda.generic_name | |
| manufacturer name | Zhejiang Jingwei Pharmaceutical Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 55621-001-01 | openfda.package_ndc |
| ndc | product | 55621-001 | openfda.product_ndc |
| ndc11 | package | 55621000101 | derived:openfda.package_ndc |
| rxcui | 106258 | openfda.rxcui | |
| spl id | 08849eb4-ae6b-8151-e063-6394a90a5a7e | id | |
| spl set id | bcc99e5a-2403-46da-9c9d-8411fa4104e0 | 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.