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Zeel
Zeel - 50114-2733-3 - (SILICON DIOXIDE and COMFREY ROOT and ARNICA MONTANA ROOT and TOXICODENDRON PUBESCENS LEAF and SULFUR and SANGUINARIA CANADENSIS ROOT and SOLANUM DULCAMARA STEM and COENZYME A and NADIDE and SODIUM DIETHYL OXALACETATE and .ALPHA.-LIPOIC ACID and SUS SCROFA CARTILAGE and SUS SCROFA EMBRYO and SUS SCROFA UMBILICAL CORD and SUS SCROFA PLACENTA and)
Drug Information of Zeel
| Product NDC: | 50114-2733 |
| Proprietary Name: | Zeel |
| Non Proprietary Name: | SILICON DIOXIDE and COMFREY ROOT and ARNICA MONTANA ROOT and TOXICODENDRON PUBESCENS LEAF and SULFUR and SANGUINARIA CANADENSIS ROOT and SOLANUM DULCAMARA STEM and COENZYME A and NADIDE and SODIUM DIETHYL OXALACETATE and .ALPHA.-LIPOIC ACID and SUS SCROFA CARTILAGE and SUS SCROFA EMBRYO and SUS SCROFA UMBILICAL CORD and SUS SCROFA PLACENTA and |
| Active Ingredient(s): | 6; 2; 6; 8; 6; 2; 6; 6; 2; 6; 2; 2; 2; 2; 2 [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g & nbsp; SILICON DIOXIDE and COMFREY ROOT and ARNICA MONTANA ROOT and TOXICODENDRON PUBESCENS LEAF and SULFUR and SANGUINARIA CANADENSIS ROOT and SOLANUM DULCAMARA STEM and COENZYME A and NADIDE and SODIUM DIETHYL OXALACETATE and .ALPHA.-LIPOIC ACID and SUS SCROFA CARTILAGE and SUS SCROFA EMBRYO and SUS SCROFA UMBILICAL CORD and SUS SCROFA PLACENTA and |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zeel
| Product NDC: | 50114-2733 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111020 |
Package Information of Zeel
| Package NDC: | 50114-2733-3 |
| Package Description: | 1 TUBE in 1 CARTON (50114-2733-3) > 50 g in 1 TUBE |
NDC Information of Zeel
| NDC Code | 50114-2733-3 |
| Proprietary Name | Zeel |
| Package Description | 1 TUBE in 1 CARTON (50114-2733-3) > 50 g in 1 TUBE |
| Product NDC | 50114-2733 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SILICON DIOXIDE and COMFREY ROOT and ARNICA MONTANA ROOT and TOXICODENDRON PUBESCENS LEAF and SULFUR and SANGUINARIA CANADENSIS ROOT and SOLANUM DULCAMARA STEM and COENZYME A and NADIDE and SODIUM DIETHYL OXALACETATE and .ALPHA.-LIPOIC ACID and SUS SCROFA CARTILAGE and SUS SCROFA EMBRYO and SUS SCROFA UMBILICAL CORD and SUS SCROFA PLACENTA and |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111020 |
| 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 STEM; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF |
| Strength Number | 6; 2; 6; 8; 6; 2; 6; 6; 2; 6; 2; 2; 2; 2; 2 |
| Strength Unit | [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g; [hp_X]/50g |
| Pharmaceutical Classes |
