Label: ALCOSCRUB FOAM liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 55863-431-02, 55863-431-32 - Packager: Erie Scientific, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated July 18, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PURPOSE
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INDICATIONS & USAGE
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.
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
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.
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALCOSCRUB FOAM
alcoscrub foam liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55863-431 Route of Administration Topical Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 1 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55863-431-02 50 mL in 1 BOTTLE 2 NDC:55863-431-32 950 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/12/2006 Labeler - Erie Scientific, LLC (361605223)
