NDC 62795-1010 – BHI Arthritis

Arnica Montana Root 6 [hp_X]/1; Berberis Vulgaris Root Bark 8 [hp_X]/1; Bryonia Alba Whole 4 [hp_X]/1; Causticum 4 [hp_X]/1; Citrullus Colocynthis Fruit Pulp 5… · Tablet · Oral

Human Otc Drug

Product NDC62795-1010

Product details

Brand name
BHI Arthritis
Generic name
ARNICA MONTANA ROOT, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA WHOLE, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, FERROSOFERRIC PHOSPHATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RANUNCULUS BULBOSUS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF , and SULFUR
Labeler
MediNatura Inc
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
January 1, 2015
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for BHI Arthritis →

Package NDC codes (2)

Package NDCDescriptionSince
62795-1010-2100 TABLET in 1 BOTTLE (62795-1010-2)May 23, 2023
62795-1010-31 BOTTLE in 1 CARTON (62795-1010-3) / 100 TABLET in 1 BOTTLEJan 1, 2015