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Gripp-Heel
Gripp-Heel - 50114-7001-6 - (ACONITUM NAPELLUS and BRYONIA ALBA ROOT and LACHESIS MUTA VENOM and EUPATORIUM PERFOLIATUM FLOWERING TOP and PHOSPHORUS)
Drug Information of Gripp-Heel
| Product NDC: | 50114-7001 |
| Proprietary Name: | Gripp-Heel |
| Non Proprietary Name: | ACONITUM NAPELLUS and BRYONIA ALBA ROOT and LACHESIS MUTA VENOM and EUPATORIUM PERFOLIATUM FLOWERING TOP and PHOSPHORUS |
| Active Ingredient(s): | 3; 3; 2; 11; 4 [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp; ACONITUM NAPELLUS and BRYONIA ALBA ROOT and LACHESIS MUTA VENOM and EUPATORIUM PERFOLIATUM FLOWERING TOP and PHOSPHORUS |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gripp-Heel
| Product NDC: | 50114-7001 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19930131 |
Package Information of Gripp-Heel
| Package NDC: | 50114-7001-6 |
| Package Description: | 10 VIAL in 1 CARTON (50114-7001-6) > 1.1 mL in 1 VIAL |
NDC Information of Gripp-Heel
| NDC Code | 50114-7001-6 |
| Proprietary Name | Gripp-Heel |
| Package Description | 10 VIAL in 1 CARTON (50114-7001-6) > 1.1 mL in 1 VIAL |
| Product NDC | 50114-7001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACONITUM NAPELLUS and BRYONIA ALBA ROOT and LACHESIS MUTA VENOM and EUPATORIUM PERFOLIATUM FLOWERING TOP and PHOSPHORUS |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19930131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | ACONITUM NAPELLUS; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; LACHESIS MUTA VENOM; PHOSPHORUS |
| Strength Number | 3; 3; 2; 11; 4 |
| Strength Unit | [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL |
| Pharmaceutical Classes |
