NDC 68654-585

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 ID68654-585_2e007cec-4db3-4991-99df-9bf2df750dcb
NDC68654-585
Product TypeHuman Otc Drug
Proprietary NameFoamahol
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2009-09-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333
Labeler NameShare Corporation
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68654-585-13

800 mL in 1 BAG (68654-585-13)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68654-585-27 [68654058527]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-07 [68654058507]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-14 [68654058514]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-13 [68654058513]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-24 [68654058524]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-10 [68654058510]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-01 [68654058501]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-11 [68654058511]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-17 [68654058517]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-06 [68654058506]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-08 [68654058508]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-03 [68654058503]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-12 [68654058512]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-55 [68654058555]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-15 [68654058515]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-16 [68654058516]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-18 [68654058518]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-05 [68654058505]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-28 [68654058528]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 68654-585-09 [68654058509]

Foamahol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:042ee54b-9f7b-4801-b399-6581614cbadd
Manufacturer
UNII

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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