| Product NDC: | 58980-615 |
| Proprietary Name: | Arctic Relief |
| Non Proprietary Name: | Menthol and Camphor (Synthetic) |
| Active Ingredient(s): | .2268; 3.969 g/113.4g; g/113.4g & nbsp; Menthol and Camphor (Synthetic) |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58980-615 |
| Labeler Name: | Stratus Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091001 |
| Package NDC: | 58980-615-40 |
| Package Description: | 1 TUBE in 1 BOX (58980-615-40) > 113.4 g in 1 TUBE |
| NDC Code | 58980-615-40 |
| Proprietary Name | Arctic Relief |
| Package Description | 1 TUBE in 1 BOX (58980-615-40) > 113.4 g in 1 TUBE |
| Product NDC | 58980-615 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol and Camphor (Synthetic) |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Stratus Pharmaceuticals, Inc |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
| Strength Number | .2268; 3.969 |
| Strength Unit | g/113.4g; g/113.4g |
| Pharmaceutical Classes |