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Pro1tek Antiseptic Foam Hand Sanitizer - 52232-100-51 - (BENZALKONIUM CHLORIDE)

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Drug Information of Pro1tek Antiseptic Foam Hand Sanitizer

Product NDC: 52232-100
Proprietary Name: Pro1tek Antiseptic Foam Hand Sanitizer
Non Proprietary Name: BENZALKONIUM CHLORIDE
Active Ingredient(s): .13    mL/100mL & nbsp;   BENZALKONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Pro1tek Antiseptic Foam Hand Sanitizer

Product NDC: 52232-100
Labeler Name: Priority Environmental Solutions
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100629

Package Information of Pro1tek Antiseptic Foam Hand Sanitizer

Package NDC: 52232-100-51
Package Description: 550 mL in 1 BOTTLE (52232-100-51)

NDC Information of Pro1tek Antiseptic Foam Hand Sanitizer

NDC Code 52232-100-51
Proprietary Name Pro1tek Antiseptic Foam Hand Sanitizer
Package Description 550 mL in 1 BOTTLE (52232-100-51)
Product NDC 52232-100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZALKONIUM CHLORIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100629
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Priority Environmental Solutions
Substance Name BENZALKONIUM CHLORIDE
Strength Number .13
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Pro1tek Antiseptic Foam Hand Sanitizer


General Information