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FOAMING HAND SANITIZER - 63148-240-08 - (BENZALKONIUM CHLORIDE)

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Drug Information of FOAMING HAND SANITIZER

Product NDC: 63148-240
Proprietary Name: FOAMING HAND SANITIZER
Non Proprietary Name: BENZALKONIUM CHLORIDE
Active Ingredient(s): .1    mL/100mL & nbsp;   BENZALKONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of FOAMING HAND SANITIZER

Product NDC: 63148-240
Labeler Name: APOLLO HEALTH AND BEAUTY CARE
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100625

Package Information of FOAMING HAND SANITIZER

Package NDC: 63148-240-08
Package Description: 236 mL in 1 BOTTLE, PUMP (63148-240-08)

NDC Information of FOAMING HAND SANITIZER

NDC Code 63148-240-08
Proprietary Name FOAMING HAND SANITIZER
Package Description 236 mL in 1 BOTTLE, PUMP (63148-240-08)
Product NDC 63148-240
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZALKONIUM CHLORIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100625
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name APOLLO HEALTH AND BEAUTY CARE
Substance Name BENZALKONIUM CHLORIDE
Strength Number .1
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of FOAMING HAND SANITIZER


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