ACTIPREP - 0064-1011-16 - (ETHYL ALCOHOL)

Alphabetical Index


Drug Information of ACTIPREP

Product NDC: 0064-1011
Proprietary Name: ACTIPREP
Non Proprietary Name: ETHYL ALCOHOL
Active Ingredient(s): .79    mL/mL & nbsp;   ETHYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of ACTIPREP

Product NDC: 0064-1011
Labeler Name: HEALTHPOINT, LTD
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20011001

Package Information of ACTIPREP

Package NDC: 0064-1011-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC (0064-1011-16)

NDC Information of ACTIPREP

NDC Code 0064-1011-16
Proprietary Name ACTIPREP
Package Description 473 mL in 1 BOTTLE, PLASTIC (0064-1011-16)
Product NDC 0064-1011
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ETHYL ALCOHOL
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20011001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name HEALTHPOINT, LTD
Substance Name ALCOHOL
Strength Number .79
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of ACTIPREP


General Information