NDC 62742-4184

Hand Sanitizer

Ethyl Alcohol

Hand Sanitizer is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Allure Labs Inc. The primary component is Alcohol.

Product ID62742-4184_a8b0ba79-3c72-4fe0-9605-baada50cb63a
NDC62742-4184
Product TypeHuman Otc Drug
Proprietary NameHand Sanitizer
Generic NameEthyl Alcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-03-17
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameAllure Labs Inc
Substance NameALCOHOL
Active Ingredient Strength650 mg/mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 62742-4184-1

59.14 mL in 1 BOTTLE, PUMP (62742-4184-1)
Marketing Start Date2020-03-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62742-4184-1 [62742418401]

Hand Sanitizer GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-17

NDC 62742-4184-2 [62742418402]

Hand Sanitizer GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL650 mg/mL

OpenFDA Data

SPL SET ID:0a087ec3-b12f-4035-b75a-f7d92b7b3fcf
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 902574