Lytta vesicatoria

FDA Drug Profile

Lytta vesicatoria is listed in the FDA National Drug Code directory with 1 NDC code. Available dosage form: liquid.

Drug Details

Generic Name
Lytta vesicatoria
Brand Names
N/A
Application Number
Sponsor
Herbamed AG
NDC Codes
1
Dosage Forms
LIQUID
Routes
N/A
Active Ingredients
LYTTA VESICATORIA

Indications and Usage

Uses For temporary relief of pain and burning sensation associated with frequent or urgent need to urinate. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

Warnings For oral use only. Blood in urine, fever, nausea, vomiting, pain in kidney area or acute urinary retention may be serious. Consult a doctor promptly if any of these symptoms occur. Do not use if you are allergic to bee venom Stop use and ask a doctor if symptoms persist for more than 5 days, worsen or new symptoms occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.