| NDC Code | 43251-2281-1 |
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| Package Description | 200 mL in 1 BOTTLE (43251-2281-1) |
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| Product NDC | 43251-2281 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Natralia Eczema And Psoriasis |
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| Non-Proprietary Name | Sodium Borate, Graphite, Potassium Sulfate, And Sodium Chloride |
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| Dosage Form | GEL |
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| Usage | TOPICAL |
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| Start Marketing Date | 20090103 |
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| End Marketing Date | 20220831 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | LaCorium Health USA Inc. |
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| Substance Name | GRAPHITE; POTASSIUM SULFATE; SODIUM BORATE; SODIUM CHLORIDE |
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| Strength | 6; 3; 20; 12 |
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| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
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| Pharmacy Classes | Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC] |
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