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natralia
natralia - 43251-2241-2 - (Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride)
Drug Information of natralia
| Product NDC: | 43251-2241 |
| Proprietary Name: | natralia |
| Non Proprietary Name: | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
| Active Ingredient(s): | 6; 3; 20; 12 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g & nbsp; Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of natralia
| Product NDC: | 43251-2241 |
| Labeler Name: | LaCorium Health International Pty Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090301 |
Package Information of natralia
| Package NDC: | 43251-2241-2 |
| Package Description: | 1 g in 1 PACKET (43251-2241-2) |
NDC Information of natralia
| NDC Code | 43251-2241-2 |
| Proprietary Name | natralia |
| Package Description | 1 g in 1 PACKET (43251-2241-2) |
| Product NDC | 43251-2241 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090301 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | LaCorium Health International Pty Ltd |
| Substance Name | GRAPHITE; POTASSIUM SULFATE; SODIUM BORATE; SODIUM CHLORIDE |
| Strength Number | 6; 3; 20; 12 |
| Strength Unit | [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g |
| Pharmaceutical Classes |
