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Woodwards HandClens Foaming Sanitizer - 60193-200-01 - (BENZALKONIUM CHLORIDE)

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Drug Information of Woodwards HandClens Foaming Sanitizer

Product NDC: 60193-200
Proprietary Name: Woodwards HandClens Foaming Sanitizer
Non Proprietary Name: BENZALKONIUM CHLORIDE
Active Ingredient(s): 1.3    mg/mL & nbsp;   BENZALKONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Woodwards HandClens Foaming Sanitizer

Product NDC: 60193-200
Labeler Name: Pacific Word Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130603

Package Information of Woodwards HandClens Foaming Sanitizer

Package NDC: 60193-200-01
Package Description: 236 mL in 1 BOTTLE, PUMP (60193-200-01)

NDC Information of Woodwards HandClens Foaming Sanitizer

NDC Code 60193-200-01
Proprietary Name Woodwards HandClens Foaming Sanitizer
Package Description 236 mL in 1 BOTTLE, PUMP (60193-200-01)
Product NDC 60193-200
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZALKONIUM CHLORIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20130603
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Pacific Word Corporation
Substance Name BENZALKONIUM CHLORIDE
Strength Number 1.3
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Woodwards HandClens Foaming Sanitizer


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