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Hand Sanitizer - 51785-424-01 - (BENZALKONIUM CHLORIDE)

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Drug Information of Hand Sanitizer

Product NDC: 51785-424
Proprietary Name: Hand Sanitizer
Non Proprietary Name: BENZALKONIUM CHLORIDE
Active Ingredient(s): .0294    g/30mL & nbsp;   BENZALKONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Hand Sanitizer

Product NDC: 51785-424
Labeler Name: Herbalife International of America Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120829

Package Information of Hand Sanitizer

Package NDC: 51785-424-01
Package Description: 30 mL in 1 BOTTLE, SPRAY (51785-424-01)

NDC Information of Hand Sanitizer

NDC Code 51785-424-01
Proprietary Name Hand Sanitizer
Package Description 30 mL in 1 BOTTLE, SPRAY (51785-424-01)
Product NDC 51785-424
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZALKONIUM CHLORIDE
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20120829
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Herbalife International of America Inc.
Substance Name BENZALKONIUM CHLORIDE
Strength Number .0294
Strength Unit g/30mL
Pharmaceutical Classes

Complete Information of Hand Sanitizer


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