NDC 44911-0659 – Spinapar

Horse Chestnut 4 [hp_X]/mL; Harpagophytum Procumbens Root 4 [hp_X]/mL; Phytolacca Americana Root 4 [hp_X]/mL; Ruta Graveolens Flowering Top 4 [hp_X]/mL; Sus… · Liquid · Oral

Human Otc Drug

Product NDC44911-0659

Product details

Brand name
Spinapar
Generic name
Aesculus Hippocastanum, Harpagophytum, Phytolacca Decandra, Ruta Graveolens, Cartilago Suis, Discus Intervertebralis suis, Agaricus Muscarius, Argentum Metallicum, Arnica Montana, Bambusa Arundinacea, Bellis Perennis, Bryonia (Alba), Calcarea Fluorica, Hypericum Perforatum, Rhus Tox, Sulphur, Tellurium Metallicum
Labeler
Energique, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
October 11, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Spinapar →

Package NDC codes (1)

Package NDCDescriptionSince
44911-0659-130 mL in 1 BOTTLE, DROPPER (44911-0659-1)Oct 11, 2022