Label: CUSTOM QUEST HAND SANITIZER- alcohol liquid

  • 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 April 8, 2020

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient[s]

    Alcohol 70%v/v

  • Purpose

    Antiseptic

  • Use[s]

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Flammable, Keep away from heat or flame.

    Do not use

    • on infants
    • on open skin wounds

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor If irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply as needed into palm of hand and thoroughly spread on both hands, rub until dry.
    • Supervise children under 6 years of age when using this product.
  • Other information

    • Store between 15-30°C(59-86°F)
    • Avoid freezing and excessive heat above 40°C(104°F)
  • INACTIVE INGREDIENT

    Inactive ingredients: Deionized water, Triethanolamine, Carbomer, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl
    Acetate

  • SPL UNCLASSIFIED SECTION

    Kills 99.9% of Germs

    Antibacterial

    with soothing ALOE VERA

    Distributed by:

    Custom Quest, Inc

    6511 West Chester Rd.

    West Chester, OH 45069

    MADE IN CHINA

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    CUSTOM QUEST HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74876-651
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74876-651-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/08/2020
    2NDC:74876-651-16500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/08/2020
    Labeler - Custom Quest, Inc. (049451540)