Lachesis mutus
LACHESIS MUTA VENOM
ORAL
HUMAN OTC DRUG
Lachesis mutus is an FDA drug label for the active ingredient LACHESIS MUTA VENOM manufactured by Boiron 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 20231113.
- Generic name
- LACHESIS MUTA VENOM
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-3012
- Application
- N/A
- Label effective
- 20231113
Active ingredients
Lachesis mutus 5C (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Hot flashes associated with menopause*
Dosage & Administration
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Contraindications
Not available.
Warnings
Not available.
Adverse Reactions
Not available.