| Product NDC: | 57520-0712 | 
| Proprietary Name: | Loma Lux Psoriasis | 
| Non Proprietary Name: | Kali bromatum, Natrum sulphuricum, 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 sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum, | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 57520-0712 | 
| Labeler Name: | Apotheca Company | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC | 
| Start Marketing Date: | 20110705 | 
| Package NDC: | 57520-0712-3 | 
| Package Description: | 1 CARTON in 1 CARTON (57520-0712-3) > 1 BOTTLE in 1 CARTON (57520-0712-2) > 237 mL in 1 BOTTLE (57520-0712-1) | 
| NDC Code | 57520-0712-3 | 
| Proprietary Name | Loma Lux Psoriasis | 
| Package Description | 1 CARTON in 1 CARTON (57520-0712-3) > 1 BOTTLE in 1 CARTON (57520-0712-2) > 237 mL in 1 BOTTLE (57520-0712-1) | 
| Product NDC | 57520-0712 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Kali bromatum, Natrum sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum, | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20110705 | 
| 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 |