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HAND SANITIZER - 57817-200-14 - (ALCOHOL)

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Drug Information of HAND SANITIZER

Product NDC: 57817-200
Proprietary Name: HAND SANITIZER
Non Proprietary Name: ALCOHOL
Active Ingredient(s): 62    mL/100mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of HAND SANITIZER

Product NDC: 57817-200
Labeler Name: Hangzhou Haorun Technology CO.,LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130330

Package Information of HAND SANITIZER

Package NDC: 57817-200-14
Package Description: 200 mL in 1 BOTTLE, PLASTIC (57817-200-14)

NDC Information of HAND SANITIZER

NDC Code 57817-200-14
Proprietary Name HAND SANITIZER
Package Description 200 mL in 1 BOTTLE, PLASTIC (57817-200-14)
Product NDC 57817-200
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20130330
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Hangzhou Haorun Technology CO.,LTD.
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of HAND SANITIZER


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