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BaniFlu
BaniFlu - 68703-035-80 - (Gelsemium, Influenzinum, Nux vom)
Drug Information of BaniFlu
| Product NDC: | 68703-035 |
| Proprietary Name: | BaniFlu |
| Non Proprietary Name: | Gelsemium, Influenzinum, Nux vom |
| Active Ingredient(s): | 30; 30; 30; 30; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp; Gelsemium, Influenzinum, Nux vom |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BaniFlu
| Product NDC: | 68703-035 |
| Labeler Name: | Native Remedies, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130102 |
Package Information of BaniFlu
| Package NDC: | 68703-035-80 |
| Package Description: | 180 TABLET in 1 BOTTLE, GLASS (68703-035-80) |
NDC Information of BaniFlu
| NDC Code | 68703-035-80 |
| Proprietary Name | BaniFlu |
| Package Description | 180 TABLET in 1 BOTTLE, GLASS (68703-035-80) |
| Product NDC | 68703-035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Gelsemium, Influenzinum, Nux vom |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130102 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Native Remedies, LLC |
| Substance Name | GELSEMIUM SEMPERVIRENS ROOT; INFLUENZA A VIRUS A/NEW CALEDONIA/20/99 (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED); INFLUENZA A VIRUS A/PANAMA/2007/99 (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED); INFLUENZA B VIRUS B/HONG KONG/330/2001 ANTIGEN (PROPIOLACTONE INACTIVATED); STRYCHNOS NUX-VOMICA SEED |
| Strength Number | 30; 30; 30; 30; 30 |
| Strength Unit | [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 |
| Pharmaceutical Classes |
