Product NDC: | 50421-002 |
Proprietary Name: | Camphor, Menthol |
Non Proprietary Name: | Camphor, Menthol |
Active Ingredient(s): | 3.4; 8.5 g/85g; g/85g & nbsp; Camphor, Menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50421-002 |
Labeler Name: | Active & Innovative Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100113 |
Package NDC: | 50421-002-13 |
Package Description: | 85 g in 1 BOTTLE, WITH APPLICATOR (50421-002-13) |
NDC Code | 50421-002-13 |
Proprietary Name | Camphor, Menthol |
Package Description | 85 g in 1 BOTTLE, WITH APPLICATOR (50421-002-13) |
Product NDC | 50421-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Camphor, Menthol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100113 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Active & Innovative Inc. |
Substance Name | CAMPHOR; MENTHOL |
Strength Number | 3.4; 8.5 |
Strength Unit | g/85g; g/85g |
Pharmaceutical Classes |