Product NDC: | 51452-003 |
Proprietary Name: | Cold Spot |
Non Proprietary Name: | menthol |
Active Ingredient(s): | 6 mL/60mL & nbsp; menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51452-003 |
Labeler Name: | Fabrication Enterprises |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100824 |
Package NDC: | 51452-003-16 |
Package Description: | 480 mL in 1 BOTTLE, SPRAY (51452-003-16) |
NDC Code | 51452-003-16 |
Proprietary Name | Cold Spot |
Package Description | 480 mL in 1 BOTTLE, SPRAY (51452-003-16) |
Product NDC | 51452-003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | menthol |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20100824 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Fabrication Enterprises |
Substance Name | MENTHOL |
Strength Number | 6 |
Strength Unit | mL/60mL |
Pharmaceutical Classes |