Psorizide Ultra - Potassium Bromide, Nickel Sulfate, and Zinc Bromide
Navigation: NDC > Supplier starting with: P > PLYMOUTH PHARMACEUTICALS INC DBA LOMA LUX LABORATORIES| Field | Value |
|---|---|
| NDC Code: | 61480-124 |
| Proprietary Name: | Psorizide Ultra |
| Suffix: | |
| Non-Proprietary Name: | Potassium Bromide, Nickel Sulfate, and Zinc Bromide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-10-1997 |
| Category Name: | UNAPPROVED HOMEOPATHIC |
| Application Number: | |
| Labeler: | PLYMOUTH PHARMACEUTICALS INC DBA LOMA LUX LABORATORIES |
| Substance Name: | NICKEL SULFATE; POTASSIUM BROMIDE; ZINC BROMIDE |
| Active Numerator Strength: | 1; 1; 4 |
| Active Ingredient Unit: | [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharm Classes: | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |
| DEA Schedule: |