Product NDC: | 63029-703 |
Proprietary Name: | New Skin Bandage |
Non Proprietary Name: | Benzethonium Chloride |
Active Ingredient(s): | .06 mg/mL & nbsp; Benzethonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63029-703 |
Labeler Name: | Medtech Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110301 |
Package NDC: | 63029-703-01 |
Package Description: | 1 JAR in 1 BOX (63029-703-01) > 30 mL in 1 JAR |
NDC Code | 63029-703-01 |
Proprietary Name | New Skin Bandage |
Package Description | 1 JAR in 1 BOX (63029-703-01) > 30 mL in 1 JAR |
Product NDC | 63029-703 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzethonium Chloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Medtech Products Inc. |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | .06 |
Strength Unit | mg/mL |
Pharmaceutical Classes |