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Mysotrol No Rinse Antiseptic Hand Cleanser - 25382-505-04 - (Ethyl Alcohol)

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Drug Information of Mysotrol No Rinse Antiseptic Hand Cleanser

Product NDC: 25382-505
Proprietary Name: Mysotrol No Rinse Antiseptic Hand Cleanser
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 62    mL/100mL & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Mysotrol No Rinse Antiseptic Hand Cleanser

Product NDC: 25382-505
Labeler Name: Derma Sciences
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20061201

Package Information of Mysotrol No Rinse Antiseptic Hand Cleanser

Package NDC: 25382-505-04
Package Description: 118 mL in 1 BOTTLE (25382-505-04)

NDC Information of Mysotrol No Rinse Antiseptic Hand Cleanser

NDC Code 25382-505-04
Proprietary Name Mysotrol No Rinse Antiseptic Hand Cleanser
Package Description 118 mL in 1 BOTTLE (25382-505-04)
Product NDC 25382-505
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20061201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Derma Sciences
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Mysotrol No Rinse Antiseptic Hand Cleanser


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