Product NDC: | 43251-3213 |
Proprietary Name: | Natralia Cramp Relief |
Non Proprietary Name: | Methyl Salicylate |
Active Ingredient(s): | 105 mg/g & nbsp; Methyl Salicylate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43251-3213 |
Labeler Name: | Laderma Trading Pty Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090301 |
Package NDC: | 43251-3213-4 |
Package Description: | 3 g in 1 PACKET (43251-3213-4) |
NDC Code | 43251-3213-4 |
Proprietary Name | Natralia Cramp Relief |
Package Description | 3 g in 1 PACKET (43251-3213-4) |
Product NDC | 43251-3213 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Methyl Salicylate |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20090301 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Laderma Trading Pty Ltd |
Substance Name | METHYL SALICYLATE |
Strength Number | 105 |
Strength Unit | mg/g |
Pharmaceutical Classes |