| Product NDC: | 75990-7008 |
| Proprietary Name: | Certus Sting Relief Prep Pad |
| Non Proprietary Name: | BENZOCAINE |
| Active Ingredient(s): | .06 mL/mL & nbsp; BENZOCAINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SWAB |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75990-7008 |
| Labeler Name: | Certus Medical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110501 |
| Package NDC: | 75990-7008-3 |
| Package Description: | .6 mL in 1 POUCH (75990-7008-3) |
| NDC Code | 75990-7008-3 |
| Proprietary Name | Certus Sting Relief Prep Pad |
| Package Description | .6 mL in 1 POUCH (75990-7008-3) |
| Product NDC | 75990-7008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOCAINE |
| Dosage Form Name | SWAB |
| Route Name | TOPICAL |
| Start Marketing Date | 20110501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Certus Medical, Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | .06 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |