Scorodite Prunus

FDA Drug Profile — Scorodite Prunus

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

Drug Details

Generic Name
Scorodite Prunus
Brand Names
Scorodite Prunus
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
CAMPHOR (NATURAL), VERATRUM ALBUM ROOT, SLOE, FERROUS ARSENATE, BOS TAURUS PITUITARY GLAND, GOLD

Indications and Usage

Directions: FOR ORAL USE ONLY.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditons worsen or persist. If pregnant or nursing consult a doctor before use.