Label: ANTIMICROBIAL HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 51811-362-21 - Packager: Hanover Pen Corp dba HPC Global
- This is a repackaged label.
- Source NDC Code(s): 61010-111
- 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 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 gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51811-362(NDC:61010-111) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 19.66 mL in 29.57 mL Inactive Ingredients Ingredient Name Strength Trolamine (UNII: 9O3K93S3TK) Aloe (UNII: V5VD430YW9) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51811-362-21 29.57 mL in 1 BOTTLE, PLASTIC 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