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Sani
Sani - 62672-608-11 - (ALCOHOL)
Drug Information of Sani
| Product NDC: | 62672-608 |
| Proprietary Name: | Sani |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sani
| Product NDC: | 62672-608 |
| Labeler Name: | Osceola Supply, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030701 |
Package Information of Sani
| Package NDC: | 62672-608-11 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (62672-608-11) |
NDC Information of Sani
| NDC Code | 62672-608-11 |
| Proprietary Name | Sani |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (62672-608-11) |
| Product NDC | 62672-608 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20030701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Osceola Supply, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
