Product NDC: | 62011-0169 |
Proprietary Name: | Earwax Removal Kit |
Non Proprietary Name: | Earwax Removal Kit |
Active Ingredient(s): | 6.5 mg/100mL & nbsp; Earwax Removal Kit |
Administration Route(s): | AURICULAR (OTIC) |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62011-0169 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part344 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120206 |
Package NDC: | 62011-0169-1 |
Package Description: | 15 mL in 1 BOTTLE (62011-0169-1) |
NDC Code | 62011-0169-1 |
Proprietary Name | Earwax Removal Kit |
Package Description | 15 mL in 1 BOTTLE (62011-0169-1) |
Product NDC | 62011-0169 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Earwax Removal Kit |
Dosage Form Name | LIQUID |
Route Name | AURICULAR (OTIC) |
Start Marketing Date | 20120206 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | CARBAMIDE PEROXIDE |
Strength Number | 6.5 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |