OHM Menopause
OHM Menopause is an FDA drug label for the active ingredient AMMONIUM CARBONICUM, AMYL NITROSUM, CIMICIFUGA RACEMOSA, GLONOINUM, LACHESIS MUTUS, SANGUINARIA, CANADENSIS. manufactured by OHM PHARMA INC. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20211229.
- Generic name
- AMMONIUM CARBONICUM, AMYL NITROSUM, CIMICIFUGA RACEMOSA, GLONOINUM, LACHESIS MUTUS, SANGUINARIA, CANADENSIS.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 66096-156
- Application
- N/A
- Label effective
- 20211229
Active ingredients
Indications & Usage
USES: Temporarily relieves symptoms caused by common menopause, hormonal imbalances. ** This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.
Dosage & Administration
DIRECTIONS: Shake 10 times before use. Hold close to mouth and spray 3 times directly under the tongue 2-3 times a day, or as directed by a health care professional. Not for use by children.
Contraindications
Not available.
Warnings
WARNINGS: IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor KEEP OUT OF REACH OF CHILDREN.
Adverse Reactions
Not available.