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 |