Zeel - 50114-6165-2 - (.ALPHA.-LIPOIC ACID, ARNICA MONTANA ROOT, SUS SCROFA CARTILAGE, COENZYME A, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE, SULFUR and COMFREY ROOT)

Alphabetical Index


Drug Information of Zeel

Product NDC: 50114-6165
Proprietary Name: Zeel
Non Proprietary Name: .ALPHA.-LIPOIC ACID, ARNICA MONTANA ROOT, SUS SCROFA CARTILAGE, COENZYME A, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE, SULFUR and COMFREY ROOT
Active Ingredient(s): 6; 1; 6; 8; 6; 3; 6; 6; 2; 6; 4; 4; 4; 4; 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; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   .ALPHA.-LIPOIC ACID, ARNICA MONTANA ROOT, SUS SCROFA CARTILAGE, COENZYME A, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE, SULFUR and COMFREY ROOT
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zeel

Product NDC: 50114-6165
Labeler Name: Heel Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130618

Package Information of Zeel

Package NDC: 50114-6165-2
Package Description: 100 TABLET in 1 BOTTLE (50114-6165-2)

NDC Information of Zeel

NDC Code 50114-6165-2
Proprietary Name Zeel
Package Description 100 TABLET in 1 BOTTLE (50114-6165-2)
Product NDC 50114-6165
Product Type Name HUMAN OTC DRUG
Non Proprietary Name .ALPHA.-LIPOIC ACID, ARNICA MONTANA ROOT, SUS SCROFA CARTILAGE, COENZYME A, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE, SULFUR and COMFREY ROOT
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130618
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc.
Substance Name .ALPHA.-LIPOIC ACID; ARNICA MONTANA ROOT; COENZYME A; COMFREY ROOT; NADIDE; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF
Strength Number 6; 1; 6; 8; 6; 3; 6; 6; 2; 6; 4; 4; 4; 4; 1
Strength Unit [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; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of Zeel


General Information