adverse reactions
ADVERSE REACTIONS: The following local adverse reactions have been reported with corticosteroid suppositories; burning, itching, irritation, dryness, folliculitis, hypopigmentation, allergic contact dermatitis, secondary infection.
Hemmorex-HC
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
- Hemmorex-HC
- Generic name
- HYDROCORTISONE ACETATE
- Manufacturer
- Laser Pharmaceuticals, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- db67f724-c78c-4280-9c2e-6abbaeaef42d
- SPL ID
- 2c65695c-de02-6fa3-e063-6294a90aee9d
- Version
- 9
- Effective date
- 2025-01-23
- 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 06:37:00
| Harmonized routes |
|---|
| RECTAL |
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 |
|---|---|---|---|
| brand name | Hemmorex-HC | openfda.brand_name | |
| generic name | HYDROCORTISONE ACETATE | openfda.generic_name | |
| manufacturer name | Laser Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 16477-201-24 | openfda.package_ndc |
| ndc | package | 16477-201-99 | openfda.package_ndc |
| ndc | package | 16477-201-12 | openfda.package_ndc |
| ndc | product | 16477-201 | openfda.product_ndc |
| ndc11 | package | 16477020124 | derived:openfda.package_ndc |
| ndc11 | package | 16477020112 | derived:openfda.package_ndc |
| ndc11 | package | 16477020199 | derived:openfda.package_ndc |
| rxcui | 1674197 | openfda.rxcui | |
| rxcui | 1291082 | openfda.rxcui | |
| spl id | 2c65695c-de02-6fa3-e063-6294a90aee9d | id | |
| spl set id | db67f724-c78c-4280-9c2e-6abbaeaef42d | set_id | |
| unii | 3X7931PO74 | openfda.unii |
Adverse reactions 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.