Crotalus horridus

CROTALUS HORRIDUS HORRIDUS VENOM ORAL HUMAN PRESCRIPTION DRUG

Crotalus horridus is an FDA drug label for the active ingredient CROTALUS HORRIDUS HORRIDUS 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
CROTALUS HORRIDUS HORRIDUS VENOM
Manufacturer
Boiron
Product type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Dosage form
N/A
NDC
0220-1577
Application
N/A
Label effective
20231113

Active ingredients

Crotalus horridus 6C (**contains 0.443 mg of the active ingredient per pellet)

Indications & Usage

Rx Only*

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.