Product NDC: | 11527-062 |
Proprietary Name: | Sheffield Pain Relief |
Non Proprietary Name: | BENZOCAINE |
Active Ingredient(s): | 200 mg/g & nbsp; BENZOCAINE |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11527-062 |
Labeler Name: | Faria LLC dba Sheffield Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20060130 |
Package NDC: | 11527-062-55 |
Package Description: | 1 TUBE in 1 CARTON (11527-062-55) > 9.35 g in 1 TUBE |
NDC Code | 11527-062-55 |
Proprietary Name | Sheffield Pain Relief |
Package Description | 1 TUBE in 1 CARTON (11527-062-55) > 9.35 g in 1 TUBE |
Product NDC | 11527-062 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZOCAINE |
Dosage Form Name | GEL |
Route Name | ORAL |
Start Marketing Date | 20060130 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Faria LLC dba Sheffield Pharmaceuticals |
Substance Name | BENZOCAINE |
Strength Number | 200 |
Strength Unit | mg/g |
Pharmaceutical Classes |