Product NDC: | 32472-102 |
Proprietary Name: | Analgesic |
Non Proprietary Name: | menthol |
Active Ingredient(s): | 700 mL/L & nbsp; menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 32472-102 |
Labeler Name: | Premiere Enterprises |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101228 |
Package NDC: | 32472-102-03 |
Package Description: | .088 L in 1 BOTTLE (32472-102-03) |
NDC Code | 32472-102-03 |
Proprietary Name | Analgesic |
Package Description | .088 L in 1 BOTTLE (32472-102-03) |
Product NDC | 32472-102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | menthol |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20101228 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Premiere Enterprises |
Substance Name | MENTHOL |
Strength Number | 700 |
Strength Unit | mL/L |
Pharmaceutical Classes |