Spongia Aurum

FDA Drug Profile — Spongia Aurum

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

Drug Details

Generic Name
Spongia Aurum
Brand Names
Spongia Aurum
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
PELLET
Routes
ORAL
Active Ingredients
PRUNUS SPINOSA FLOWER BUD, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, GOLD, CALCIUM CARBONATE, SUGARCANE, SPONGIA OFFICINALIS SKELETON, ROASTED

Indications and Usage

Directions: FOR ORAL USE ONLY.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.