Product NDC: | 68703-039 |
Proprietary Name: | BrightSpark |
Non Proprietary Name: | Arg nit, Arsenicum iod, Hyoscyamus, Veratrum alb |
Active Ingredient(s): | 30; 30; 6; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp; Arg nit, Arsenicum iod, Hyoscyamus, Veratrum alb |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68703-039 |
Labeler Name: | Native Remedies, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20121004 |
Package NDC: | 68703-039-80 |
Package Description: | 180 TABLET in 1 BOTTLE, GLASS (68703-039-80) |
NDC Code | 68703-039-80 |
Proprietary Name | BrightSpark |
Package Description | 180 TABLET in 1 BOTTLE, GLASS (68703-039-80) |
Product NDC | 68703-039 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Arg nit, Arsenicum iod, Hyoscyamus, Veratrum alb |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121004 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Native Remedies, LLC |
Substance Name | ARSENIC TRIIODIDE; HYOSCYAMUS NIGER; SILVER NITRATE; VERATRUM ALBUM ROOT |
Strength Number | 30; 30; 6; 30 |
Strength Unit | [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 |
Pharmaceutical Classes |