ANEMONE PRATENSIS

FDA Drug Profile

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

Drug Details

Generic Name
ANEMONE PRATENSIS
Brand Names
N/A
Application Number
Sponsor
Herbamed AG
NDC Codes
1
Dosage Forms
LIQUID
Routes
N/A
Active Ingredients
ANEMONE PRATENSIS

Indications and Usage

INDICATIONS Inability to control urination.

Warnings

Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.