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 |