Label: QUIK SPRAY- advanced hand sanitizing spray spray

  • 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 4, 2009

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  • ACTIVE INGREDIENT

    Drug Facts

    Active Ingredients                              Purpose

    Ethyl Alcohol 62 percent                   Antimicrobial

    Triclosan 0.3 percent                        Antimicrobial

  • PURPOSE

    Uses

    For hand washing to decrease bacteria on the skin,

    recommended for repeated use.

  • WARNINGS

    Warnings

    For external use on the hands only. Flammable.

    Keep away from heat and flame. Keep out if reach of children.

    Stop use and ask doctor if irritation develops.

  • DOSAGE & ADMINISTRATION

    Directions

    Wet hands thoroughly with product and allow to dry without wiping.

    Not recommended for infants.

  • INACTIVE INGREDIENT

    Aloe Barbadensis Extract , Deionized Water ,  Hydroxyehylcellulose , PEG  40 Hydrogenated Castor Oil ,

    Perfume , Propylene Glycol , Tocopherol

  • DESCRIPTION

    Net Wt 8mL 0.27 FL OZ Made in China

    Dist by Nupak, LLC 5823 Bowen Daniek Dr. 1601 Tampa FL 33616 1 888 988 7232

  • PRINCIPAL DISPLAY PANEL

    6 Hour Germ Protection

    QuikSpray

    90 plus sprays

    Advanced Hand Sanitizing Spray

    www.myquikspray.net

    Contains Aloes Vera and Vitamin E

    Kills 99.99 percent of germs

  • PRINCIPAL DISPLAY PANEL

    QuikSpray24Pieces

  • INGREDIENTS AND APPEARANCE
    QUIK SPRAY 
    advanced hand sanitizing spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41900-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.03 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41900-500-0224 in 1 BOX
    1NDC:41900-500-018 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33310/01/2009
    Labeler - Cinogen Cosmetics Zhaoqing, LTD. (527929812)
    Registrant - Cinogen Cosmetics Zhaoqing, LTD. (527929812)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cinogen Cosmetics Zhaoqing, LTD.527929812manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Nupak LLC826963550import
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