Loma Lux Psoriasis is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Apotheca Company. The primary component is Potassium Bromide; Sodium Bromide; Nickel Sulfate Hexahydrate; Potassium Sulfate; Zinc Bromide.
| Product ID | 57520-0713_a4b3c89c-c5f6-4ca7-ad45-72942c86e512 |
| NDC | 57520-0713 |
| Product Type | Human Otc Drug |
| Proprietary Name | Loma Lux Psoriasis |
| Generic Name | Kali Bromatum, Natrum Bromatum, Niccolum Sulphuricum, Kali Sulphuricum, Zincum Bromatum, |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-07-07 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | POTASSIUM BROMIDE; SODIUM BROMIDE; NICKEL SULFATE HEXAHYDRATE; POTASSIUM SULFATE; ZINC BROMIDE |
| Active Ingredient Strength | 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2011-07-07 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-07-07 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-07-07 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-07-07 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| POTASSIUM BROMIDE | 1 [hp_X]/mL |
| SPL SET ID: | 1b88d668-388b-43b0-b968-eda35d536191 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 57520-0712 | Loma Lux Psoriasis | Kali bromatum, Natrum sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum, |
| 57520-0713 | Loma Lux Psoriasis | Kali bromatum, Natrum bromatum, Niccolum sulphuricum, Kali sulphuricum, Zincum bromatum, |