warnings
Warnings For rectal use only
iShancare Hemorrhoid and Fissure Cream
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
- iShancare Hemorrhoid and Fissure Cream
- Generic name
- ISHANCARE HEMORRHOID CREAM
- Manufacturer
- Shenzhen Ishan Technology Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 570775ce-a1ed-e57d-e063-6394a90aeeff
- SPL ID
- 570775df-a7f5-e5cf-e063-6394a90aab96
- Version
- 1
- Effective date
- 2026-07-20
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:50:18
| 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 |
|---|---|---|---|
| brand name | iShancare Hemorrhoid and Fissure Cream | openfda.brand_name | |
| generic name | ISHANCARE HEMORRHOID CREAM | openfda.generic_name | |
| manufacturer name | Shenzhen Ishan Technology Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 73076-189-01 | openfda.package_ndc |
| ndc | product | 73076-189 | openfda.product_ndc |
| ndc11 | package | 73076018901 | derived:openfda.package_ndc |
| spl id | 570775df-a7f5-e5cf-e063-6394a90aab96 | id | |
| spl set id | 570775ce-a1ed-e57d-e063-6394a90aeeff | set_id | |
| unii | 4T6H12BN9U | 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.