Product NDC: | 51452-001 |
Proprietary Name: | Cold Spot |
Non Proprietary Name: | menthol, methyl salicylate |
Active Ingredient(s): | .46; .15 L/3.8L; L/3.8L & nbsp; menthol, methyl salicylate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51452-001 |
Labeler Name: | Fabrication Enterprises |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100824 |
Package NDC: | 51452-001-32 |
Package Description: | 960 mL in 1 BOTTLE (51452-001-32) |
NDC Code | 51452-001-32 |
Proprietary Name | Cold Spot |
Package Description | 960 mL in 1 BOTTLE (51452-001-32) |
Product NDC | 51452-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | menthol, methyl salicylate |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100824 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Fabrication Enterprises |
Substance Name | MENTHOL; METHYL SALICYLATE |
Strength Number | .46; .15 |
Strength Unit | L/3.8L; L/3.8L |
Pharmaceutical Classes |