Product NDC: | 57520-0272 |
Proprietary Name: | Fibro Relief |
Non Proprietary Name: | Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica |
Active Ingredient(s): | 30; 30; 30; 30; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp; Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57520-0272 |
Labeler Name: | Apotheca Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20101217 |
Package NDC: | 57520-0272-1 |
Package Description: | 120 CAPSULE in 1 BOTTLE (57520-0272-1) |
NDC Code | 57520-0272-1 |
Proprietary Name | Fibro Relief |
Package Description | 120 CAPSULE in 1 BOTTLE (57520-0272-1) |
Product NDC | 57520-0272 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20101217 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Apotheca Company |
Substance Name | GUAIACUM OFFICINALE RESIN; IRON; LITHIUM CARBONATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; TOMATO |
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 |