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Allure Isopropyl Rubbing Alcohol
Allure Isopropyl Rubbing Alcohol - 52000-001-06 - (Isopropyl Alcohol)
Drug Information of Allure Isopropyl Rubbing Alcohol
| Product NDC: | 52000-001 |
| Proprietary Name: | Allure Isopropyl Rubbing Alcohol |
| Non Proprietary Name: | Isopropyl Alcohol |
| Active Ingredient(s): | 50 mL/100mL & nbsp; Isopropyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allure Isopropyl Rubbing Alcohol
| Product NDC: | 52000-001 |
| Labeler Name: | Universal Distribution Center LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120629 |
Package Information of Allure Isopropyl Rubbing Alcohol
| Package NDC: | 52000-001-06 |
| Package Description: | 414 mL in 1 BOTTLE, PLASTIC (52000-001-06) |
NDC Information of Allure Isopropyl Rubbing Alcohol
| NDC Code | 52000-001-06 |
| Proprietary Name | Allure Isopropyl Rubbing Alcohol |
| Package Description | 414 mL in 1 BOTTLE, PLASTIC (52000-001-06) |
| Product NDC | 52000-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Isopropyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120629 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Universal Distribution Center LLC |
| Substance Name | ISOPROPYL ALCOHOL |
| Strength Number | 50 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
