Product NDC: | 57520-0713 |
Proprietary Name: | Loma Lux Psoriasis |
Non Proprietary Name: | Kali bromatum, Natrum bromatum, Niccolum sulphuricum, Kali sulphuricum, Zincum bromatum, |
Active Ingredient(s): | 3; 1; 4; 2; 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Kali bromatum, Natrum bromatum, Niccolum sulphuricum, Kali sulphuricum, Zincum bromatum, |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57520-0713 |
Labeler Name: | Apotheca Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20110707 |
Package NDC: | 57520-0713-3 |
Package Description: | 1 CARTON in 1 CARTON (57520-0713-3) > 1 BOTTLE in 1 CARTON (57520-0713-2) > 237 mL in 1 BOTTLE (57520-0713-1) |
NDC Code | 57520-0713-3 |
Proprietary Name | Loma Lux Psoriasis |
Package Description | 1 CARTON in 1 CARTON (57520-0713-3) > 1 BOTTLE in 1 CARTON (57520-0713-2) > 237 mL in 1 BOTTLE (57520-0713-1) |
Product NDC | 57520-0713 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Kali bromatum, Natrum bromatum, Niccolum sulphuricum, Kali sulphuricum, Zincum bromatum, |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110707 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Apotheca Company |
Substance Name | NICKEL SULFATE HEXAHYDRATE; POTASSIUM BROMIDE; POTASSIUM SULFATE; SODIUM BROMIDE; ZINC BROMIDE |
Strength Number | 3; 1; 4; 2; 4 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |