Product NDC: | 41167-0053 |
Proprietary Name: | Benzodent |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | .2 g/g & nbsp; Benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41167-0053 |
Labeler Name: | Chattem, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19940512 |
Package NDC: | 41167-0053-4 |
Package Description: | 1 TUBE in 1 CARTON (41167-0053-4) > 28 g in 1 TUBE |
NDC Code | 41167-0053-4 |
Proprietary Name | Benzodent |
Package Description | 1 TUBE in 1 CARTON (41167-0053-4) > 28 g in 1 TUBE |
Product NDC | 41167-0053 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19940512 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Chattem, Inc. |
Substance Name | BENZOCAINE |
Strength Number | .2 |
Strength Unit | g/g |
Pharmaceutical Classes |