Product NDC: | 63029-322 |
Proprietary Name: | DEBROX |
Non Proprietary Name: | Carbamide Peroxide |
Active Ingredient(s): | .065 mg/mL & nbsp; Carbamide Peroxide |
Administration Route(s): | AURICULAR (OTIC) |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63029-322 |
Labeler Name: | Medtech Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part344 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120601 |
Package NDC: | 63029-322-02 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (63029-322-02) > 7 mL in 1 BOTTLE, DROPPER |
NDC Code | 63029-322-02 |
Proprietary Name | DEBROX |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (63029-322-02) > 7 mL in 1 BOTTLE, DROPPER |
Product NDC | 63029-322 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Carbamide Peroxide |
Dosage Form Name | LIQUID |
Route Name | AURICULAR (OTIC) |
Start Marketing Date | 20120601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medtech Products Inc. |
Substance Name | CARBAMIDE PEROXIDE |
Strength Number | .065 |
Strength Unit | mg/mL |
Pharmaceutical Classes |