NDC 62742-4185

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 ID62742-4185_468e7a1b-0a5a-491c-82f1-7b62de68fe2e
NDC62742-4185
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 Strength700 mg/mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 62742-4185-1

473 mL in 1 BOTTLE, PUMP (62742-4185-1)
Marketing Start Date2020-03-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62742-4185-2 [62742418502]

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

NDC 62742-4185-1 [62742418501]

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

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL700 mg/mL

OpenFDA Data

SPL SET ID:726f53c6-c12d-4e11-838d-8de0058100ef
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581662