NDC 64578-0101 – Endocrinpath

Alfalfa 15 [hp_X]/mL; Borage 15 [hp_X]/mL; Oyster Shell Calcium Carbonate, Crude 15 [hp_X]/mL; Ceanothus Americanus Leaf 4 [hp_X]/mL; Anhydrous Citric Acid 15… · Liquid · Oral

Human Otc Drug

Product NDC64578-0101

Product details

Brand name
Endocrinpath
Generic name
Alfalfa, Borago Officinalis, Calcarea Carbonica, Ceanothus Americanus, Citricum Acidum, Fucus Vesiculosus, Ginkgo Biloba, Glandula Suprarenalis Suis, Glycyrrhiza Glabra, Hydrocotyle Asiatica, Hypothalamus (Bovine), Kali Phosphoricum, Pancreas Suis, Phytolacca Decandra, Pituitarum Posterium (Bovine), Sarsaparilla (Smilax Regelii), Silicea, Syzygium Jambolanum, Taraxacum Officinale, Thyroidinum (Bovine)
Labeler
Energetix Corporation
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
November 20, 2014
Listing expires
December 31, 2026
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Endocrinpath →

Package NDC codes (1)

Package NDCDescriptionSince
64578-0101-159.1 mL in 1 BOTTLE, DROPPER (64578-0101-1)Mar 24, 2016