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Hand Sanitizer - 75887-001-04 - (ALCOHOL)

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Drug Information of Hand Sanitizer

Product NDC: 75887-001
Proprietary Name: Hand Sanitizer
Non Proprietary Name: ALCOHOL
Active Ingredient(s): 5    mL/8mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Hand Sanitizer

Product NDC: 75887-001
Labeler Name: Aztex Enterprises
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110118

Package Information of Hand Sanitizer

Package NDC: 75887-001-04
Package Description: 118 mL in 1 BOTTLE (75887-001-04)

NDC Information of Hand Sanitizer

NDC Code 75887-001-04
Proprietary Name Hand Sanitizer
Package Description 118 mL in 1 BOTTLE (75887-001-04)
Product NDC 75887-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110118
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Aztex Enterprises
Substance Name ALCOHOL
Strength Number 5
Strength Unit mL/8mL
Pharmaceutical Classes

Complete Information of Hand Sanitizer


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