Home > National Drug Code (NDC) > Arthritis Relief

Arthritis Relief - 61727-302-21 - (ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF)

Alphabetical Index


Drug Information of Arthritis Relief

Product NDC: 61727-302
Proprietary Name: Arthritis Relief
Non Proprietary Name: ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF
Active Ingredient(s): 18; 8; 8; 8; 8; 8    [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp;   ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Arthritis Relief

Product NDC: 61727-302
Labeler Name: Homeocare Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120731

Package Information of Arthritis Relief

Package NDC: 61727-302-21
Package Description: 4 g in 1 TUBE (61727-302-21)

NDC Information of Arthritis Relief

NDC Code 61727-302-21
Proprietary Name Arthritis Relief
Package Description 4 g in 1 TUBE (61727-302-21)
Product NDC 61727-302
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20120731
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Homeocare Laboratories
Substance Name ARNICA MONTANA; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM; KALMIA LATIFOLIA LEAF; MATRICARIA RECUTITA; TOXICODENDRON PUBESCENS LEAF
Strength Number 18; 8; 8; 8; 8; 8
Strength Unit [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g
Pharmaceutical Classes

Complete Information of Arthritis Relief


General Information