warnings
Warnings
Cyclease Menopause
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
- Cyclease Menopause
- Generic name
- ARNICA MONTANA WHOLE, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SANGUINARIA CANADENSIS ROOT
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a227e8d8-27a3-592f-e053-2a95a90ab31c
- SPL ID
- 030b038f-d916-dc07-e063-6394a90a6e5e
- Version
- 3
- Effective date
- 2023-08-16
- Source export date
- 2026-11-06
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 08:11:25
| Harmonized routes |
|---|
| ORAL |
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 | Cyclease Menopause | openfda.brand_name | |
| generic name | ARNICA MONTANA WHOLE, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SANGUINARIA CANADENSIS ROOT | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9082-04 | openfda.package_ndc |
| ndc | product | 0220-9082 | openfda.product_ndc |
| ndc11 | package | 00220908204 | derived:openfda.package_ndc |
| spl id | 030b038f-d916-dc07-e063-6394a90a6e5e | id | |
| spl set id | a227e8d8-27a3-592f-e053-2a95a90ab31c | set_id | |
| unii | O80TY208ZW | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | G59M7S0WS3 | openfda.unii | |
| unii | N9288CD508 | openfda.unii | |
| unii | K73E24S6X9 | 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.