Product NDC: | 0573-0225 |
Proprietary Name: | ANBESOL MAXIMUM STRENGTH GEL |
Non Proprietary Name: | benzocaine |
Active Ingredient(s): | 200 mg/g & nbsp; benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-0225 |
Labeler Name: | Wyeth Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20050511 |
Package NDC: | 0573-0225-67 |
Package Description: | 1 TUBE in 1 BLISTER PACK (0573-0225-67) > 9 g in 1 TUBE |
NDC Code | 0573-0225-67 |
Proprietary Name | ANBESOL MAXIMUM STRENGTH GEL |
Package Description | 1 TUBE in 1 BLISTER PACK (0573-0225-67) > 9 g in 1 TUBE |
Product NDC | 0573-0225 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzocaine |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20050511 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Wyeth Consumer Healthcare |
Substance Name | BENZOCAINE |
Strength Number | 200 |
Strength Unit | mg/g |
Pharmaceutical Classes |