Label: INSTANT HAND SANITIZER UNSCENTED WITH MOISTURIZER AND VITAMIN E- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 50154-5000-2, 50154-5000-8 - Packager: Lantern Enterprises Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 May 27, 2010
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- STORAGE AND HANDLING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- WHEN USING
- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INSTANT HAND SANITIZER UNSCENTED WITH MOISTURIZER AND VITAMIN E
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50154-5000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SULISOBENZONE (UNII: 1W6L629B4K) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) MANNITOL (UNII: 3OWL53L36A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50154-5000-2 59 mL in 1 BOTTLE 2 NDC:50154-5000-8 236 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 05/27/2010 Labeler - Lantern Enterprises Ltd (240084249) Establishment Name Address ID/FEI Business Operations Lantern Science Shenzhen Co. Ltd 421252423 manufacture