| 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 |