Product NDC: | 50114-1195 |
Proprietary Name: | Belladonna Homaccord |
Non Proprietary Name: | ATROPA BELLADONNA and ECHINACEA, UNSPECIFIED |
Active Ingredient(s): | 3; 10 [hp_X]/50mL; [hp_X]/50mL & nbsp; ATROPA BELLADONNA and ECHINACEA, UNSPECIFIED |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-1195 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19860131 |
Package NDC: | 50114-1195-4 |
Package Description: | 50 mL in 1 BOTTLE (50114-1195-4) |
NDC Code | 50114-1195-4 |
Proprietary Name | Belladonna Homaccord |
Package Description | 50 mL in 1 BOTTLE (50114-1195-4) |
Product NDC | 50114-1195 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ATROPA BELLADONNA and ECHINACEA, UNSPECIFIED |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19860131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | ATROPA BELLADONNA; ECHINACEA, UNSPECIFIED |
Strength Number | 3; 10 |
Strength Unit | [hp_X]/50mL; [hp_X]/50mL |
Pharmaceutical Classes |