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Antibacterial Foaming Hand - 50988-293-00 - (Benzalkonium Chloride)

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Drug Information of Antibacterial Foaming Hand

Product NDC: 50988-293
Proprietary Name: Antibacterial Foaming Hand
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): .325    mL/295.74mL & nbsp;   Benzalkonium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Antibacterial Foaming Hand

Product NDC: 50988-293
Labeler Name: Jets, Sets, & Elephants Beauty Corp.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120125

Package Information of Antibacterial Foaming Hand

Package NDC: 50988-293-00
Package Description: 295.74 mL in 1 BOTTLE, PUMP (50988-293-00)

NDC Information of Antibacterial Foaming Hand

NDC Code 50988-293-00
Proprietary Name Antibacterial Foaming Hand
Package Description 295.74 mL in 1 BOTTLE, PUMP (50988-293-00)
Product NDC 50988-293
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium Chloride
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20120125
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Jets, Sets, & Elephants Beauty Corp.
Substance Name BENZALKONIUM CHLORIDE
Strength Number .325
Strength Unit mL/295.74mL
Pharmaceutical Classes

Complete Information of Antibacterial Foaming Hand


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