| 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: | 51452-001-04 |
| Package Description: | 120 mL in 1 TUBE (51452-001-04) |
| NDC Code | 51452-001-04 |
| Proprietary Name | Cold Spot |
| Package Description | 120 mL in 1 TUBE (51452-001-04) |
| 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 |