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SaniFoam
SaniFoam - 52030-773-25 - (ALCOHOL)
Drug Information of SaniFoam
| Product NDC: | 52030-773 |
| Proprietary Name: | SaniFoam |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | 620 mg/g & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SaniFoam
| Product NDC: | 52030-773 |
| Labeler Name: | Genesan Systems |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100101 |
Package Information of SaniFoam
| Package NDC: | 52030-773-25 |
| Package Description: | 199 g in 1 CAN (52030-773-25) |
NDC Information of SaniFoam
| NDC Code | 52030-773-25 |
| Proprietary Name | SaniFoam |
| Package Description | 199 g in 1 CAN (52030-773-25) |
| Product NDC | 52030-773 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Genesan Systems |
| Substance Name | ALCOHOL |
| Strength Number | 620 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
