"44911-0139-1" National Drug Code (NDC)

NDC Code	44911-0139-1
Package Description	57 g in 1 TUBE (44911-0139-1)
Product NDC	44911-0139
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Arthritis
Proprietary Name Suffix	Gel
Non-Proprietary Name	Colchicum Autumnale, Propolis, Kalmia Latifolia, Bronia (alba), Causticum, Kali Carbonicum, Ledum Palustre, Rhododendron Chrysanthum, Rhus Tox, Thuja Occidentalis
Dosage Form	GEL
Usage	TOPICAL
Start Marketing Date	20150202
End Marketing Date	20220623
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Energique, Inc.
Substance Name	BRYONIA ALBA ROOT; CAUSTICUM; COLCHICUM AUTUMNALE BULB; KALMIA LATIFOLIA LEAF; LEDUM PALUSTRE TWIG; POTASSIUM CARBONATE; PROPOLIS WAX; RHODODENDRON AUREUM LEAF; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF
Strength	12; 12; 6; 6; 12; 12; 6; 12; 12; 12
Strength Unit	[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g