| Product NDC: | 63830-855 | 
| Proprietary Name: | Prevent | 
| Non Proprietary Name: | ALCOHOL | 
| Active Ingredient(s): | .62 mL/mL & nbsp; ALCOHOL | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63830-855 | 
| Labeler Name: | Pro Chem, Incorporated | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333E | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20090901 | 
| Package NDC: | 63830-855-10 | 
| Package Description: | 1000 mL in 1 CARTRIDGE (63830-855-10) | 
| NDC Code | 63830-855-10 | 
| Proprietary Name | Prevent | 
| Package Description | 1000 mL in 1 CARTRIDGE (63830-855-10) | 
| Product NDC | 63830-855 | 
| 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 | .62 | 
| Strength Unit | mL/mL | 
| Pharmaceutical Classes |