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Hand Sanitizer - 61734-085-09 - (Ethyl Alcohol)

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Drug Information of Hand Sanitizer

Product NDC: 61734-085
Proprietary Name: Hand Sanitizer
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 62    mg/117.6mL & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Hand Sanitizer

Product NDC: 61734-085
Labeler Name: Delon Laboratories (1990) Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20101001

Package Information of Hand Sanitizer

Package NDC: 61734-085-09
Package Description: 725 mL in 1 BOTTLE, PLASTIC (61734-085-09)

NDC Information of Hand Sanitizer

NDC Code 61734-085-09
Proprietary Name Hand Sanitizer
Package Description 725 mL in 1 BOTTLE, PLASTIC (61734-085-09)
Product NDC 61734-085
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20101001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Delon Laboratories (1990) Ltd
Substance Name ALCOHOL
Strength Number 62
Strength Unit mg/117.6mL
Pharmaceutical Classes

Complete Information of Hand Sanitizer


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