Label: ANTIMICROBIAL HAND SANITIZER- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 51811-353-25 - Packager: Hanover Pen Corp dba HPC Global
- Category: HUMAN OTC DRUG LABEL
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 September 13, 2010
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- WARNINGS
- DO NOT USE
- STOP USE
- Keep out of reach of children.
- Directions
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIMICROBIAL HAND SANITIZER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51811-353 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 2.79 mL in 4.5 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51811-353-25 4.5 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/13/2010 Labeler - Hanover Pen Corp dba HPC Global (003022670) Establishment Name Address ID/FEI Business Operations Hanover Pen Corp dba HPC Global 003022670 repack, label Establishment Name Address ID/FEI Business Operations Bell Pharmaceuticals 140653770 manufacture