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Auro-Dri
Auro-Dri - 63736-327-12 - (Isopropyl Alcohol)
Drug Information of Auro-Dri
| Product NDC: | 63736-327 |
| Proprietary Name: | Auro-Dri |
| Non Proprietary Name: | Isopropyl Alcohol |
| Active Ingredient(s): | 28 mL/29mL & nbsp; Isopropyl Alcohol |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Auro-Dri
| Product NDC: | 63736-327 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part344 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100614 |
Package Information of Auro-Dri
| Package NDC: | 63736-327-12 |
| Package Description: | 12 BOX in 1 CASE (63736-327-12) > 1 BOTTLE in 1 BOX > 29 mL in 1 BOTTLE |
NDC Information of Auro-Dri
| NDC Code | 63736-327-12 |
| Proprietary Name | Auro-Dri |
| Package Description | 12 BOX in 1 CASE (63736-327-12) > 1 BOTTLE in 1 BOX > 29 mL in 1 BOTTLE |
| Product NDC | 63736-327 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Isopropyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20100614 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | ISOPROPYL ALCOHOL |
| Strength Number | 28 |
| Strength Unit | mL/29mL |
| Pharmaceutical Classes |
