warnings
for external use only when using finger cots or an applicator, apply externally or to the skin of the anal canal only do not put this product into the rectum
WowDay 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
- WowDay Hemorrhoid and Fissure Cream
- Generic name
- HEMORRHOID AND FISSURE CREAM
- Manufacturer
- WowDay LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 47ba86ad-240a-e733-e063-6394a90a24e3
- SPL ID
- 4aa59584-e9b1-1f3f-e063-6394a90aeb21
- Version
- 2
- Effective date
- 2026-02-12
- Source export date
- 2026-10-27
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:50:51
| 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 |
|---|---|---|---|
| application number | M015 | openfda.application_number | |
| brand name | WowDay Hemorrhoid and Fissure Cream | openfda.brand_name | |
| generic name | HEMORRHOID AND FISSURE CREAM | openfda.generic_name | |
| manufacturer name | WowDay LLC | openfda.manufacturer_name | |
| ndc | package | 87113-1008-1 | openfda.package_ndc |
| ndc | product | 87113-1008 | openfda.product_ndc |
| ndc11 | package | 87113100801 | derived:openfda.package_ndc |
| rxcui | 2734148 | openfda.rxcui | |
| spl id | 4aa59584-e9b1-1f3f-e063-6394a90aeb21 | id | |
| spl set id | 47ba86ad-240a-e733-e063-6394a90a24e3 | set_id | |
| unii | 101I4J0U34 | openfda.unii | |
| unii | PDC6A3C0OX | openfda.unii | |
| unii | L7T10EIP3A | 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.