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Skintegrity Foaming Hand Sanitizer - 53329-975-82 - (Ethyl Alcohol)

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Drug Information of Skintegrity Foaming Hand Sanitizer

Product NDC: 53329-975
Proprietary Name: Skintegrity Foaming Hand Sanitizer
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 62    mL/100mL & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Skintegrity Foaming Hand Sanitizer

Product NDC: 53329-975
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110408

Package Information of Skintegrity Foaming Hand Sanitizer

Package NDC: 53329-975-82
Package Description: 50 mL in 1 BOTTLE, PUMP (53329-975-82)

NDC Information of Skintegrity Foaming Hand Sanitizer

NDC Code 53329-975-82
Proprietary Name Skintegrity Foaming Hand Sanitizer
Package Description 50 mL in 1 BOTTLE, PUMP (53329-975-82)
Product NDC 53329-975
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20110408
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Medline Industries, Inc.
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Skintegrity Foaming Hand Sanitizer


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