Product NDC: | 43251-3323 |
Proprietary Name: | natralia |
Non Proprietary Name: | SILICON DIOXIDE and SODIUM CHLORIDE |
Active Ingredient(s): | 3; 12 [hp_X]/mL; [hp_X]/mL & nbsp; SILICON DIOXIDE and SODIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43251-3323 |
Labeler Name: | LaCorium Health International Pty Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20090301 |
Package NDC: | 43251-3323-5 |
Package Description: | 200 mL in 1 BOTTLE (43251-3323-5) |
NDC Code | 43251-3323-5 |
Proprietary Name | natralia |
Package Description | 200 mL in 1 BOTTLE (43251-3323-5) |
Product NDC | 43251-3323 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SILICON DIOXIDE and SODIUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20090301 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | LaCorium Health International Pty Ltd |
Substance Name | SILICON DIOXIDE; SODIUM CHLORIDE |
Strength Number | 3; 12 |
Strength Unit | [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |