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Antibacterial Foaming Hand Sanitizer - 50988-192-00 - (Benzalkonium chloride)

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Drug Information of Antibacterial Foaming Hand Sanitizer

Product NDC: 50988-192
Proprietary Name: Antibacterial Foaming Hand Sanitizer
Non Proprietary Name: Benzalkonium chloride
Active Ingredient(s): .055    mL/50.275mL & nbsp;   Benzalkonium chloride
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Antibacterial Foaming Hand Sanitizer

Product NDC: 50988-192
Labeler Name: Jets, Sets, & Elephants Beauty Corp.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100803

Package Information of Antibacterial Foaming Hand Sanitizer

Package NDC: 50988-192-00
Package Description: 50.275 mL in 1 BOTTLE, PUMP (50988-192-00)

NDC Information of Antibacterial Foaming Hand Sanitizer

NDC Code 50988-192-00
Proprietary Name Antibacterial Foaming Hand Sanitizer
Package Description 50.275 mL in 1 BOTTLE, PUMP (50988-192-00)
Product NDC 50988-192
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium chloride
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20100803
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Jets, Sets, & Elephants Beauty Corp.
Substance Name BENZALKONIUM CHLORIDE
Strength Number .055
Strength Unit mL/50.275mL
Pharmaceutical Classes

Complete Information of Antibacterial Foaming Hand Sanitizer


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