Product NDC: | 68647-120 |
Proprietary Name: | BaniFlu |
Non Proprietary Name: | Influenzinum , Bacillinum , Gelsemium , Lactose |
Active Ingredient(s): | 30; 30; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp; Influenzinum , Bacillinum , Gelsemium , Lactose |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68647-120 |
Labeler Name: | Feelgood Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20100719 |
Package NDC: | 68647-120-10 |
Package Description: | 125 TABLET in 1 BOTTLE, GLASS (68647-120-10) |
NDC Code | 68647-120-10 |
Proprietary Name | BaniFlu |
Package Description | 125 TABLET in 1 BOTTLE, GLASS (68647-120-10) |
Product NDC | 68647-120 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Influenzinum , Bacillinum , Gelsemium , Lactose |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100719 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Feelgood Health |
Substance Name | ESCHERICHIA COLI; GELSEMIUM SEMPERVIRENS ROOT; HAEMOPHILUS INFLUENZAE TYPE B |
Strength Number | 30; 30; 30 |
Strength Unit | [hp_C]/1; [hp_C]/1; [hp_C]/1 |
Pharmaceutical Classes |