Label: INSTANT HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 49959-1111-0 - Packager: Graphic Controls
- 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 November 9, 2009
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Pupose
- Uses
- Warnings
- Keep out of reach of children
- Directions
- Inactive ingredients
- PACKAGE LABEL - PRINCIPAL DISPLAY PANEL – BOTTLE
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INGREDIENTS AND APPEARANCE
INSTANT HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49959-1111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol .60 g in 1 mL Inactive Ingredients Ingredient Name Strength Aloe (UNII: V5VD430YW9) D&C Green No. 5 (UNII: 8J6RDU8L9X) D&C Yellow No. 10 (UNII: 35SW5USQ3G) Water (UNII: 059QF0KO0R) Product Characteristics Color green (green) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49959-1111-0 59 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 11/30/2009 Labeler - Graphic Controls (002111896) Registrant - Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc 874965262 MANUFACTURE