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 | 57520-0712_4cefb645-9980-44f7-8e11-794448d38366 |
| NDC | 57520-0712 |
| Product Type | Human Otc Drug |
| Proprietary Name | Loma Lux Psoriasis |
| Generic Name | Kali Bromatum, Natrum Sulphuricum, Niccolum Sulphuricum, Kali Sulphuricum, Zincum Bromatum, |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-07-05 |
| 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 | 2011-07-05 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-07-05 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-07-05 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-07-05 |
| Ingredient | Strength |
|---|---|
| POTASSIUM BROMIDE | 1 [hp_X]/mL |
| SPL SET ID: | 06616a68-5a01-4a8f-9269-6c28825cf0a7 |
| 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, |