Label: INSTANT HAND SANITIZER - STRAWBERRY SCENTED- alcohol liquid

  • 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 November 3, 2011

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  • Drug Facts


  • Active ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antimicrobial

  • Uses

    • for handwashing to decrease bacteria on the skin
    • recommended for repeated use
  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

    in the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation and redness develop and persist for more than 72 hours.


    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet hands thoroughly with product
    • briskly rub hands together until dry
    • supervise children in the use of this product
  • Other information

    • store at 20 degrees to 25 degrees C (68 degrees to 77 degrees F)
    • may discolor certain fabrics
  • Inactive ingredients:

    aloe vera leaf juice, carbomer,fd c no.33,  fragrance, glycerin, propylene glycol, tocpheryl acetate, triethanolamine, water.

  • DISTRIBUTED BY: GREENBRIER INTERNATIONAL, INC. CHESAPEAKE, VA 23320 MADE IN CHINA


  • Instant Hand Sanitizer Extra Enriched With Vitamin E Bead Strawberry Scented 2 Piece Pack Inner Label (10586-9105-2)

    InnerStrawberryLabel1

    InnerStrawberryLabel2

  • Instant Hand Sanitizer Extra Enriched With Vitamin E Bead Strawberry Scented 2 Piece Pack Outer Label (10586-9105-2)


    OuterStrawberryLabel1

    OuterStrawberryLabel2

  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER - STRAWBERRY SCENTED 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10586-9105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10586-9105-22 in 1 PACKAGE
    160 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333E11/02/2011
    Labeler - Core Brands, Inc. (184543135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Unichem Household Products Co., Ltd.528196956manufacture
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