ALCOSCRUB FOAM- alcoscrub foam liquid 
Erie Scientific, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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AlcoScrub Foam

Ethyl Alcohol 62% v/v

DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin, Water

Use as part of your daily cleaning routine. Apply a small amount to palm. Rub product into hands and allow to dry.

Antiseptic Cleanser. Effective in destroying certain bacteria and removing impurities to provide antiseptic cleansing.

Antiseptic cleanser. Use as part of your daily cleaning routine.

Flammable. Keep away from open flame and sources of heat. Avoid contact with eyes.

Discontinue use and ask a health practitioner if irritation develops. If swallowed seek medical help or contact Posion Control immediately. Keep out of reach of children.

If swallowed seek medical help or contact Posion Control immediately.

For external use only.

Flammable. Keep away from open flame and sources of heat.

Avoid contact with eyes. If contact occurs, flush eyes with water.

Discontinue use and ask a health practitioner if irritation develops.

If swallowed seek medical help or contact Posion Control immediately.

Keep out of reach of children.

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ALCOSCRUB FOAM 
alcoscrub foam liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55863-431
Route of AdministrationTopical
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL1 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55863-431-0250 mL in 1 BOTTLE
2NDC:55863-431-32950 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/12/2006
Labeler - Erie Scientific, LLC (361605223)

Revised: 7/2013
Document Id: 9f9a0274-9fb4-4a96-b036-20ff1295c1f3
Set id: 49c46ff7-5d08-4607-ad36-4f44afa3b7bc
Version: 1
Effective Time: 20130718
 
Erie Scientific, LLC