NDC 55863-431

Alcoscrub Foam

Alcoscrub Foam

Alcoscrub Foam is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Erie Scientific, Llc. The primary component is Alcohol.

Product ID55863-431_9f9a0274-9fb4-4a96-b036-20ff1295c1f3
NDC55863-431
Product TypeHuman Otc Drug
Proprietary NameAlcoscrub Foam
Generic NameAlcoscrub Foam
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2006-01-12
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameErie Scientific, LLC
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 55863-431-32

950 mL in 1 BOTTLE (55863-431-32)
Marketing Start Date2006-01-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55863-431-32 [55863043132]

Alcoscrub Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-01-12
Inactivation Date2019-11-27

NDC 55863-431-02 [55863043102]

Alcoscrub Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-01-12
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL1 mL/mL

OpenFDA Data

SPL SET ID:49c46ff7-5d08-4607-ad36-4f44afa3b7bc
Manufacturer
UNII
UPC Code
  • 0355863433206
  • 0355863430205

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