warnings
Warnings Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Menopause Relief
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
- Menopause Relief
- Generic name
- AMYL NIT, CALC CARB, CAULOPHYLLUM, CIMICIFUGA, FERRUM MET, GELSEMIUM, LACHESIS, PULSATILLA, SANGUINARIA, SEPIA, SULPHUR AND SULPHURICUM AC.
- Manufacturer
- King Bio Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e12b75f5-6c5f-4b39-a6aa-dad07089f1d8
- SPL ID
- 6fdc80e5-9b13-4bc0-b1da-305fdcb98463
- Version
- 1
- Effective date
- 2026-03-10
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:26:38
| 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 | Menopause Relief | openfda.brand_name | |
| generic name | AMYL NIT, CALC CARB, CAULOPHYLLUM, CIMICIFUGA, FERRUM MET, GELSEMIUM, LACHESIS, PULSATILLA, SANGUINARIA, SEPIA, SULPHUR AND SULPHURICUM AC. | openfda.generic_name | |
| manufacturer name | King Bio Inc. | openfda.manufacturer_name | |
| ndc | package | 57955-9973-2 | openfda.package_ndc |
| ndc | product | 57955-9973 | openfda.product_ndc |
| ndc11 | package | 57955997302 | derived:openfda.package_ndc |
| spl id | 6fdc80e5-9b13-4bc0-b1da-305fdcb98463 | id | |
| spl set id | e12b75f5-6c5f-4b39-a6aa-dad07089f1d8 | set_id | |
| unii | JTJ6HH6YEH | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | O40UQP6WCF | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | E1UOL152H7 | openfda.unii | |
| unii | N9288CD508 | openfda.unii | |
| unii | I76KB35JEV | openfda.unii | |
| unii | 22T8Z09XAK | 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.