NDC 62795-1010

BHI Arthritis

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

BHI Arthritis is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Medinatura Inc. The primary component is 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; Sulfur.

Product ID62795-1010_3dc42410-9d02-4dd7-bdd6-ee36f7acca10
NDC62795-1010
Product TypeHuman Otc Drug
Proprietary NameBHI Arthritis
Generic NameArnica 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
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMediNatura Inc
Substance NameARNICA 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; SULFUR
Active Ingredient Strength6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 62795-1010-3

1 BOTTLE in 1 CARTON (62795-1010-3) > 100 TABLET in 1 BOTTLE
Marketing Start Date2015-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62795-1010-2 [62795101002]

BHI Arthritis TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-01

Drug Details


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