Label: INSTANTFOAM ALCOHOL HAND SANITIZER- ethyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 11084-017-01, 11084-017-27, 11084-017-40 - Packager: Deb USA, Inc.
- 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 August 19, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INSTANTFOAM ALCOHOL HAND SANITIZER
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 72 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) Propyl Alcohol (UNII: 96F264O9SV) Behentrimonium Chloride (UNII: X7GNG3S47T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-017-01 47 mL in 1 BOTTLE, PUMP 2 NDC:11084-017-40 400 mL in 1 BOTTLE, SPRAY 3 NDC:11084-017-27 1000 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 06/02/2008 Labeler - Deb USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations Deb Worldwide Healthcare Inc. 205662831 manufacture
