| 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 |