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Foamahol
Foamahol - 68654-585-07 - (ALCOHOL)
Drug Information of Foamahol
| Product NDC: | 68654-585 |
| Proprietary Name: | Foamahol |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Foamahol
| Product NDC: | 68654-585 |
| Labeler Name: | Share Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
Package Information of Foamahol
| Package NDC: | 68654-585-07 |
| Package Description: | 700 mL in 1 BAG (68654-585-07) |
NDC Information of Foamahol
| NDC Code | 68654-585-07 |
| Proprietary Name | Foamahol |
| Package Description | 700 mL in 1 BAG (68654-585-07) |
| Product NDC | 68654-585 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Share Corporation |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
