| 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 |