NDC 21749-965

ETHYL ALCOHOL

Alcohol

ETHYL ALCOHOL is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Gojo Industries, Inc.. The primary component is Alcohol.

Product ID21749-965_b58960cc-d5d2-47c4-b866-2b1f8fc2709f
NDC21749-965
Product TypeHuman Otc Drug
Proprietary NameETHYL ALCOHOL
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2010-03-15
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameGOJO Industries, Inc.
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 21749-965-04

118 mL in 1 BOTTLE (21749-965-04)
Marketing Start Date2010-03-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21749-965-12 [21749096512]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-08 [21749096508]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-33 [21749096533]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15

NDC 21749-965-59 [21749096559]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-05 [21749096505]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-80 [21749096580]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-02 [21749096502]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-04 [21749096504]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-67 [21749096567]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-20 [21749096520]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-03-15
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

NDC 21749-965-10 [21749096510]

ETHYL ALCOHOL GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-26
Marketing End Date2019-12-23
Inactivation Date2019-10-21
Reactivation Date2019-12-23

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.62 mL/mL

OpenFDA Data

SPL SET ID:c7df89ae-7e2b-40b0-b3d0-e3cd7d70c683
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581660

    • NDC Crossover Matching brand name "ETHYL ALCOHOL" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    68345-652ETHYL ALCOHOLETHYL ALCOHOL
    21749-506ETHYL ALCOHOLETHYL ALCOHOL
    21749-965ETHYL ALCOHOLETHYL ALCOHOL
    21749-967ETHYL ALCOHOLETHYL ALCOHOL
    21749-993ETHYL ALCOHOLETHYL ALCOHOL
    49035-747Ethyl AlcoholEthyl Alcohol
    49035-752Ethyl AlcoholEthyl Alcohol
    49035-988Ethyl AlcoholEthyl Alcohol
    49035-322Ethyl AlcoholEthyl Alcohol
    49035-303Ethyl AlcoholEthyl Alcohol
    49035-740Ethyl AlcoholEthyl Alcohol
    49035-993Ethyl AlcoholEthyl Alcohol
    49035-779Ethyl AlcoholEthyl Alcohol
    50730-8672ethyl alcoholethyl alcohol
    54622-015Ethyl AlcoholEthyl Alcohol
    62011-0353Ethyl AlcoholEthyl Alcohol
    62832-447Ethyl alcoholEthyl alcohol
    11344-951Ethyl AlcoholEthyl Alcohol
    49035-420Ethyl alcoholEthyl alcohol
    49035-696Ethyl alcoholEthyl alcohol
    49035-418Ethyl alcoholEthyl alcohol
    49035-867Ethyl alcoholEthyl alcohol
    49035-694Ethyl alcoholEthyl alcohol
    49035-417Ethyl AlcoholEthyl Alcohol
    73764-002Ethyl AlcoholEthyl Alcohol
    74630-8303ETHYL ALCOHOLETHYL ALCOHOL
    49283-700Ethyl AlcoholEthyl Alcohol
    73762-070Ethyl AlcoholEthyl Alcohol
    74331-080ETHYL ALCOHOLETHYL ALCOHOL
    49283-050Ethyl AlcoholEthyl Alcohol
    49283-701Ethyl AlcoholEthyl Alcohol
    0363-0370Advanced Hand SanitizerAlcohol
    0363-0046AlcoholAlcohol
    0074-9857Alcohol - Hand SanitizerAlcohol
    0065-8000Alcohol Antiseptic 80%Alcohol
    0363-0663Crisp Apple Hand SaniEthyl Alcohol
    0363-0876Ethyl Rubbing AlcoholEthyl Alcohol
    0113-7077hand sanitizerethyl alcohol
    0363-0469Hand SanitizerEthyl Alcohol
    0363-0596Hand SanitizerEthyl Alcohol
    0363-0643Hand SanitizerEthyl Alcohol
    0363-0826Hand SanitizerEthyl Alcohol
    0363-0890Hand SanitizerEthyl Alcohol
    0363-0898Hand SanitizerEthyl Alcohol
    0219-2020Humphreys Alcoholado MaravillaALCOHOL
    0295-9025Nozin Nasal SanitizerAlcohol
    0362-6000SeptoSanAlcohol
    0362-6001SeptoSanAlcohol
    0362-6002SeptoSanAlcohol
    0064-1080SURGICEPTethyl alcohol
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