Label: HAND SANITIZER- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 63926-5660-1, 63926-5660-2, 63926-5660-3, 63926-5660-4 - Packager: ProActive Solutions USA, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 31, 2014
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- DESCRIPTION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63926-5660 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 kg in 100 kg Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 10 kg in 100 kg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63926-5660-2 12.86 kg in 1 DRUM 2 NDC:63926-5660-3 16.08 kg in 1 DRUM 3 NDC:63926-5660-4 48.23 kg in 1 DRUM 4 NDC:63926-5660-1 176.85 kg in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/30/2009 Labeler - ProActive Solutions USA, LLC (089577290) Registrant - ProActive Solutions USA, LLC (089577290) Establishment Name Address ID/FEI Business Operations ProActive Solutions USA, LLC 089577290 api manufacture(63926-5660) , label(63926-5660) , pack(63926-5660) , repack(63926-5660)
