NDC 64578-0103 – Renapath

Chondrodendron Tomentosum Root 10 [hp_X]/mL; Petroselinum Crispum 4 [hp_X]/mL; Sus Scrofa Pituitary Gland 12 [hp_X]/mL; Rubia Tinctorum Root 6 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC64578-0103

Product details

Brand name
Renapath
Generic name
Benzoicum Acidum, Berberis Vulgaris, Bryonia, DNA, Eupatorium Purpureum, Glandula Suprarenalis Suis, Hydrangea Arborescens, Hypothalamus, Mercurius Corrosivus, Pancreas Suis, Pareira Brava, Petroselinum Sativum, Pituitarum Posterium, Rubia Tinctorum, Sarsaparilla, Solidago Virgaurea, Thyroidinum (Bovine), Uva-Ursi
Labeler
Energetix Corporation
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
June 6, 2014
Listing expires
December 31, 2027
Pharmacologic class
Nitrogen Binding Agent

Active ingredients

Uses, dosage, side effects and warnings for Renapath →

Package NDC codes (1)

Package NDCDescriptionSince
64578-0103-159.1 mL in 1 BOTTLE, DROPPER (64578-0103-1)Jul 13, 2017