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Isopropyl Alcohol
Isopropyl Alcohol - 70253-307-16 - (Isopropyl Alcohol)
Drug Information of Isopropyl Alcohol
| Product NDC: | 70253-307 |
| Proprietary Name: | Isopropyl Alcohol |
| Non Proprietary Name: | Isopropyl Alcohol |
| Active Ingredient(s): | 70 mL/100mL & nbsp; Isopropyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isopropyl Alcohol
| Product NDC: | 70253-307 |
| Labeler Name: | Nash Finch |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090821 |
Package Information of Isopropyl Alcohol
| Package NDC: | 70253-307-16 |
| Package Description: | 437 mL in 1 BOTTLE, PLASTIC (70253-307-16) |
NDC Information of Isopropyl Alcohol
| NDC Code | 70253-307-16 |
| Proprietary Name | Isopropyl Alcohol |
| Package Description | 437 mL in 1 BOTTLE, PLASTIC (70253-307-16) |
| Product NDC | 70253-307 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Isopropyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20090821 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Nash Finch |
| Substance Name | ISOPROPYL ALCOHOL |
| Strength Number | 70 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
