Hand-E XL - 62257-606-27 - (ALCOHOL)

Alphabetical Index

Drug Information of Hand-E XL

Product NDC: 62257-606
Proprietary Name: Hand-E XL
Non Proprietary Name: ALCOHOL
Active Ingredient(s): .7    mL/mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Hand-E XL

Product NDC: 62257-606
Labeler Name: ABC Compounding Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Start Marketing Date: 20050401

Package Information of Hand-E XL

Package NDC: 62257-606-27
Package Description: 800 mL in 1 CARTRIDGE (62257-606-27)

NDC Information of Hand-E XL

NDC Code 62257-606-27
Proprietary Name Hand-E XL
Package Description 800 mL in 1 CARTRIDGE (62257-606-27)
Product NDC 62257-606
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20050401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name ABC Compounding Co., Inc.
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Hand-E XL

General Information