Product NDC: | 50114-1064 |
Proprietary Name: | Euphorbium Compositum |
Non Proprietary Name: | PULSATILLA VULGARIS and EUPHORBIA RESINIFERA RESIN and LUFFA OPERCULATA FRUIT and MERCURIC IODIDE and SUS SCROFA NASAL MUCOSA and SILVER NITRATE and CALCIUM SULFIDE and SINUSITISINUM |
Active Ingredient(s): | 10; 4; 6; 8; 2; 10; 13; 8 [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL & nbsp; PULSATILLA VULGARIS and EUPHORBIA RESINIFERA RESIN and LUFFA OPERCULATA FRUIT and MERCURIC IODIDE and SUS SCROFA NASAL MUCOSA and SILVER NITRATE and CALCIUM SULFIDE and SINUSITISINUM |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-1064 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19930131 |
Package NDC: | 50114-1064-6 |
Package Description: | 10 VIAL in 1 CARTON (50114-1064-6) > 2.2 mL in 1 VIAL |
NDC Code | 50114-1064-6 |
Proprietary Name | Euphorbium Compositum |
Package Description | 10 VIAL in 1 CARTON (50114-1064-6) > 2.2 mL in 1 VIAL |
Product NDC | 50114-1064 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | PULSATILLA VULGARIS and EUPHORBIA RESINIFERA RESIN and LUFFA OPERCULATA FRUIT and MERCURIC IODIDE and SUS SCROFA NASAL MUCOSA and SILVER NITRATE and CALCIUM SULFIDE and SINUSITISINUM |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19930131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | CALCIUM SULFIDE; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; PULSATILLA VULGARIS; SILVER NITRATE; SINUSITISINUM; SUS SCROFA NASAL MUCOSA |
Strength Number | 10; 4; 6; 8; 2; 10; 13; 8 |
Strength Unit | [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL |
Pharmaceutical Classes |