Product NDC: | 65923-002 |
Proprietary Name: | Coralite ALCOHOL PADS |
Non Proprietary Name: | ISOPROPYL ALCOHOL |
Active Ingredient(s): | 70 mg/100mg & nbsp; ISOPROPYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65923-002 |
Labeler Name: | UNITED EXCHANGE CORP. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120114 |
Package NDC: | 65923-002-01 |
Package Description: | 30 PACKET in 1 CARTON (65923-002-01) > .6 mg in 1 PACKET |
NDC Code | 65923-002-01 |
Proprietary Name | Coralite ALCOHOL PADS |
Package Description | 30 PACKET in 1 CARTON (65923-002-01) > .6 mg in 1 PACKET |
Product NDC | 65923-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ISOPROPYL ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120114 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | UNITED EXCHANGE CORP. |
Substance Name | ISOPROPYL ALCOHOL |
Strength Number | 70 |
Strength Unit | mg/100mg |
Pharmaceutical Classes |