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Carroll Ultrex Antimicrobial Wipes - 10685-681-97 - (Benzalkonium Chloride)

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Drug Information of Carroll Ultrex Antimicrobial Wipes

Product NDC: 10685-681
Proprietary Name: Carroll Ultrex Antimicrobial Wipes
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): .01417    g/1 & nbsp;   Benzalkonium Chloride
Administration Route(s): PERCUTANEOUS
Dosage Form(s): CLOTH
Coding System: National Drug Codes(NDC)

Labeler Information of Carroll Ultrex Antimicrobial Wipes

Product NDC: 10685-681
Labeler Name: Carroll Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120915

Package Information of Carroll Ultrex Antimicrobial Wipes

Package NDC: 10685-681-97
Package Description: 70 CLOTH in 1 CANISTER (10685-681-97)

NDC Information of Carroll Ultrex Antimicrobial Wipes

NDC Code 10685-681-97
Proprietary Name Carroll Ultrex Antimicrobial Wipes
Package Description 70 CLOTH in 1 CANISTER (10685-681-97)
Product NDC 10685-681
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium Chloride
Dosage Form Name CLOTH
Route Name PERCUTANEOUS
Start Marketing Date 20120915
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Carroll Company
Substance Name BENZALKONIUM CHLORIDE
Strength Number .01417
Strength Unit g/1
Pharmaceutical Classes

Complete Information of Carroll Ultrex Antimicrobial Wipes


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