Bambusa Pulsatilla

FDA Drug Profile — Bambusa Pulsatilla

Bambusa Pulsatilla is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Bambusa Pulsatilla. Available dosage form: liquid.

Drug Details

Generic Name
Bambusa Pulsatilla
Brand Names
Bambusa Pulsatilla
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
VISCUM ALBUM FRUITING TOP, EQUISETUM ARVENSE TOP, FORMICA RUFA, PULSATILLA VULGARIS, BAMBUSA VULGARIS WHOLE, STACHYS OFFICINALIS, BOS TAURUS INTERVERTEBRAL DISC, ROSMARINUS OFFICINALIS FLOWERING TOP, TIN, FERROSOFERRIC PHOSPHATE, SILICON DIOXIDE

Indications and Usage

FOR ORAL USE ONLY

Warnings

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. Contains traces of lactose. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.