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Vanilla Hand Sanitizer - 75997-011-01 - (ETHYL ALCOHOL)

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Drug Information of Vanilla Hand Sanitizer

Product NDC: 75997-011
Proprietary Name: Vanilla Hand Sanitizer
Non Proprietary Name: ETHYL ALCOHOL
Active Ingredient(s): 62    mL/100mL & nbsp;   ETHYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Vanilla Hand Sanitizer

Product NDC: 75997-011
Labeler Name: Papermates, Inc. dba Noteworthy
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110202

Package Information of Vanilla Hand Sanitizer

Package NDC: 75997-011-01
Package Description: 59 mL in 1 BOTTLE (75997-011-01)

NDC Information of Vanilla Hand Sanitizer

NDC Code 75997-011-01
Proprietary Name Vanilla Hand Sanitizer
Package Description 59 mL in 1 BOTTLE (75997-011-01)
Product NDC 75997-011
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ETHYL ALCOHOL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110202
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Papermates, Inc. dba Noteworthy
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Vanilla Hand Sanitizer


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