NDCFind

Berberis Oxalis 48951-2161

Product NDC

48951-2161
Manufacturer
Uriel Pharmacy Inc.
Dosage Form
Liquid
Route
Oral
Product Type
Human Otc Drug
Marketing Start
September 1, 2009
Listing Expires
December 31, 2027

Active Ingredients

IngredientStrength
Berberis Vulgaris Root Bark2 [hp_X]/mL
Oxalis Stricta Whole8 [hp_X]/mL
Saw Palmetto8 [hp_X]/mL
Urtica Urens6 [hp_X]/mL
Viscum Album Fruiting Top3 [hp_X]/mL
Magnesium Sulfate, Unspecified Form10 [hp_X]/mL
Bos Taurus Prostate Gland3 [hp_X]/mL
Penoxsulam3 [hp_X]/mL
Ferric Picrate4 [hp_X]/mL

Drug Class

Calculi Dissolution Agent [EPC]Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]

Packaging Options(1)

10 AMPULE in 1 BOX (48951-2161-1) / 1 mL in 1 AMPULE