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Cyclease Cramps
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 Cramps
- Generic name
- BLACK COHOSH, CITRULLUS COLOCYNTHIS FRUIT PULP, ESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Manufacturer
- Laboratoires Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 39c20cb2-79c4-4775-b3a9-55cfa67fb743
- SPL ID
- f63ce25e-71a7-5139-e053-2a95a90af330
- Version
- 7
- Effective date
- 2023-03-06
- Source export date
- 2026-10-27
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:46:48
| 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 Cramps | openfda.brand_name | |
| generic name | BLACK COHOSH, CITRULLUS COLOCYNTHIS FRUIT PULP, ESIUM PHOSPHATE, DIBASIC TRIHYDRATE | openfda.generic_name | |
| manufacturer name | Laboratoires Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9078-04 | openfda.package_ndc |
| ndc | product | 0220-9078 | openfda.product_ndc |
| ndc11 | package | 00220907804 | derived:openfda.package_ndc |
| spl id | f63ce25e-71a7-5139-e053-2a95a90af330 | id | |
| spl set id | 39c20cb2-79c4-4775-b3a9-55cfa67fb743 | set_id | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | K73E24S6X9 | openfda.unii | |
| unii | 23H32AOH17 | 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.