Product NDC: | 68093-7037 |
Proprietary Name: | StingEze |
Non Proprietary Name: | Benzocaine, Phenol |
Active Ingredient(s): | .05; .0135 g/g; g/g & nbsp; Benzocaine, Phenol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68093-7037 |
Labeler Name: | Wisconsin Pharmacal Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090201 |
Package NDC: | 68093-7037-2 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68093-7037-2) > 14.79 g in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 68093-7037-2 |
Proprietary Name | StingEze |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68093-7037-2) > 14.79 g in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 68093-7037 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine, Phenol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20090201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Wisconsin Pharmacal Company |
Substance Name | BENZOCAINE; PHENOL |
Strength Number | .05; .0135 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |