Pulsatilla

FDA Drug Profile — Pulsatilla, Pulsatilla 200ck, Pulsatilla 200C, Pulsatilla 7131

Pulsatilla is listed in the FDA National Drug Code directory with 5 NDC codes, marketed under brand names including Pulsatilla, Pulsatilla 200ck, Pulsatilla 200C. Available dosage forms: globule, pellet, liquid.

Drug Details

Generic Name
Pulsatilla
Brand Names
Pulsatilla, Pulsatilla 200ck, Pulsatilla 200C, Pulsatilla 7131
Application Number
Sponsor
True Botanica, LLC
NDC Codes
5
Dosage Forms
GLOBULE, PELLET, LIQUID
Routes
ORAL, SUBLINGUAL
Active Ingredients
PULSATILLA VULGARIS, ANEMONE PULSATILLA, PULSATILLA ALPINA WHOLE, PULSATILLA VULGARIS WHOLE, PULSATILLA MONTANA WHOLE

Indications and Usage

USES: May temporarily relieve: •symptoms due to fatigue after the least exertion •memory issues •constipation** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: Stop use and ask a doctor if symptoms persist for more than 7 days. 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. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING Store in a cool, dry place.