NDC 68654-855

Foamahol

Alcohol

Foamahol is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Share Corporation. The primary component is Alcohol.

Product ID68654-855_7a98da8b-ae38-4a6d-b2e1-5a198f11ffd0
NDC68654-855
Product TypeHuman Otc Drug
Proprietary NameFoamahol
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2019-07-11
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameShare Corporation
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68654-855-14

3785 mL in 1 BOTTLE, PLASTIC (68654-855-14)
Marketing Start Date2019-07-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68654-855-16 [68654085516]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-12 [68654085512]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-28 [68654085528]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-10 [68654085510]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-07 [68654085507]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-05 [68654085505]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-18 [68654085518]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11

NDC 68654-855-01 [68654085501]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-27 [68654085527]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-11 [68654085511]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-03 [68654085503]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-17 [68654085517]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11

NDC 68654-855-13 [68654085513]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-09 [68654085509]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-06 [68654085506]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-14 [68654085514]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11

NDC 68654-855-24 [68654085524]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-08 [68654085508]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-55 [68654085555]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

NDC 68654-855-15 [68654085515]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-11
Marketing End Date2019-07-11

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.62 mL/mL

OpenFDA Data

SPL SET ID:7a85327e-1bf8-4824-a09d-f3c585d291a5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 616763

    • NDC Crossover Matching brand name "Foamahol" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    68654-585FoamaholFoamahol
    68654-855FoamaholFoamahol
    0363-0370Advanced Hand SanitizerAlcohol
    0363-9776Advanced Hand SanitizerAlcohol
    0363-0046AlcoholAlcohol
    0074-9857Alcohol - Hand SanitizerAlcohol
    0065-8000Alcohol Antiseptic 80%Alcohol
    0404-0122Antibacterialalcohol
    0395-0040Ethyl Rubbing AlcoholAlcohol
    0363-0968Hand SanitizerALCOHOL
    0219-2020Humphreys Alcoholado MaravillaALCOHOL
    0404-5988Instant Hand Sanitizeralcohol
    0295-9025Nozin Nasal SanitizerAlcohol
    0362-6000SeptoSanAlcohol
    0362-6001SeptoSanAlcohol
    0362-6002SeptoSanAlcohol
    0064-1050TRISEPTINALCOHOL
    0363-1305WalgreensAlcohol
    0363-1306WalgreensAlcohol
    0363-1307WalgreensAlcohol
    0363-1308WalgreensAlcohol
    0363-1309WalgreensAlcohol
    0363-0969Walgreens Advanced Hand Sanitizer Citrus ScentAlcohol
    0363-9005Walgreens Advanced Hand Sanitizer Made with Plant-Based Ethyl AlcoholAlcohol
    0363-9003Walgreens Advanced Hand Sanitizer with Aloe and Vitamin EAlcohol
    0363-0967WALGREENS ADVANCED HAND SANITIZER WITH FRESH SCENTALCOHOL
    0363-9004Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
    0363-9008Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
    0363-9006Walgreens Hand Sanitizer Coastal Breeze ScentAlcohol
    0363-9007Walgreens Hand Sanitizer Crisp Apple ScentAlcohol
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