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Prevent
Prevent - 63830-585-11 - (ALCOHOL)
Drug Information of Prevent
| Product NDC: | 63830-585 |
| Proprietary Name: | Prevent |
| 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 Prevent
| Product NDC: | 63830-585 |
| Labeler Name: | Pro Chem, Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
Package Information of Prevent
| Package NDC: | 63830-585-11 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (63830-585-11) |
NDC Information of Prevent
| NDC Code | 63830-585-11 |
| Proprietary Name | Prevent |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (63830-585-11) |
| Product NDC | 63830-585 |
| 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 | Pro Chem, Incorporated |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
