Product NDC: | 65121-003 |
Proprietary Name: | Cold Spot |
Non Proprietary Name: | menthol |
Active Ingredient(s): | 12 mL/120mL & nbsp; menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65121-003 |
Labeler Name: | Pure Source |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100824 |
Package NDC: | 65121-003-04 |
Package Description: | 120 mL in 1 BOTTLE, SPRAY (65121-003-04) |
NDC Code | 65121-003-04 |
Proprietary Name | Cold Spot |
Package Description | 120 mL in 1 BOTTLE, SPRAY (65121-003-04) |
Product NDC | 65121-003 |
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 | Pure Source |
Substance Name | MENTHOL |
Strength Number | 12 |
Strength Unit | mL/120mL |
Pharmaceutical Classes |