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Skintegrity Foaming Hand Sanitizer - 53329-976-84 - (Benzethonium Chloride)

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Drug Information of Skintegrity Foaming Hand Sanitizer

Product NDC: 53329-976
Proprietary Name: Skintegrity Foaming Hand Sanitizer
Non Proprietary Name: Benzethonium Chloride
Active Ingredient(s): .2    mL/100mL & nbsp;   Benzethonium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Skintegrity Foaming Hand Sanitizer

Product NDC: 53329-976
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: 53329-976-84
Package Description: 1000 mL in 1 BAG (53329-976-84)

NDC Information of Skintegrity Foaming Hand Sanitizer

NDC Code 53329-976-84
Proprietary Name Skintegrity Foaming Hand Sanitizer
Package Description 1000 mL in 1 BAG (53329-976-84)
Product NDC 53329-976
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzethonium Chloride
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 BENZETHONIUM CHLORIDE
Strength Number .2
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Skintegrity Foaming Hand Sanitizer


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