Natralia Eczema and Psoriasis is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Lacorium Health Usa Inc.. The primary component is Sodium Borate; Graphite; Potassium Sulfate; Sodium Chloride.
Product ID | 43251-2281_220eb2b9-79fe-4d3e-a53c-cecdfc5d01e7 |
NDC | 43251-2281 |
Product Type | Human Otc Drug |
Proprietary Name | Natralia Eczema and Psoriasis |
Generic Name | Sodium Borate, Graphite, Potassium Sulfate, And Sodium Chloride |
Dosage Form | Gel |
Route of Administration | TOPICAL |
Marketing Start Date | 2009-01-03 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | LaCorium Health USA Inc. |
Substance Name | SODIUM BORATE; GRAPHITE; POTASSIUM SULFATE; SODIUM CHLORIDE |
Active Ingredient Strength | 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2009-01-03 |
Marketing End Date | 2022-08-31 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | UNAPPROVED HOMEOPATHIC |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-01-03 |
Ingredient | Strength |
---|---|
SODIUM BORATE | 20 [hp_X]/mL |
SPL SET ID: | fb7be5dc-3d93-441b-860a-a2caa5cacb70 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
0295-9035 | Natralia Eczema and Psoriasis | Sodium Borate (20X HPUS), Graphite (6X HPUS), Potassium Sulfate (3X HPUS), Sodium Chloride (12X HPUS) |
43251-2281 | Natralia Eczema and Psoriasis | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
43251-2231 | Flexitol Naturals Eczema and Psoriasis | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
43251-2241 | natralia | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |