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Natralia Eczema and Psoriasis
Natralia Eczema and Psoriasis - 43251-2281-1 - (Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride)
Drug Information of Natralia Eczema and Psoriasis
| Product NDC: | 43251-2281 |
| Proprietary Name: | Natralia Eczema and Psoriasis |
| Non Proprietary Name: | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
| Active Ingredient(s): | 6; 3; 20; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Natralia Eczema and Psoriasis
| Product NDC: | 43251-2281 |
| Labeler Name: | LaCorium Health USA Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090103 |
Package Information of Natralia Eczema and Psoriasis
| Package NDC: | 43251-2281-1 |
| Package Description: | 200 mL in 1 BOTTLE (43251-2281-1) |
NDC Information of Natralia Eczema and Psoriasis
| NDC Code | 43251-2281-1 |
| Proprietary Name | Natralia Eczema and Psoriasis |
| Package Description | 200 mL in 1 BOTTLE (43251-2281-1) |
| Product NDC | 43251-2281 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20090103 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | LaCorium Health USA Inc. |
| Substance Name | GRAPHITE; POTASSIUM SULFATE; SODIUM BORATE; SODIUM CHLORIDE |
| Strength Number | 6; 3; 20; 12 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |
