WINTER APPLE (HAND SANITIZER) GEL [MEIJER DISTRIBUTION, INC]

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WINTER APPLE (HAND SANITIZER) GEL [MEIJER DISTRIBUTION, INC]
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NDC 41250-119-06, 41250-119-10, 41250-119-16, 41250-119-32, 41250-119-34, 41250-119-38
Set ID cea1d735-71ee-4d1f-83b8-a1003a410d73
Category HUMAN OTC DRUG LABEL
Packager Meijer Distribution, Inc
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active ingredient

    Ethyl alcohol 62%

  • Purpose

    Antiseptic  

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    For external use only: hands

    Flammable.  Keep away from fire or flame

  • When using this product

    • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest
  • Stop use and ask a doctor if

    • irritation or redness develops
    • condition persists 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 hand thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants
  • Other information

    • do not store above 105°F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, glycerin, carbomer, fragrance, red 40, red 33

  • SPL UNCLASSIFIED SECTION

    *Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds

    DISTRIBUTED BY

    MIEJER DSTRIBUTION, INC

    GRAND RAPIDS, MI 49544

    www.meijer.com

    Questions 1-999-593-0593

  • principal display panel

    meijer

    Hand Sanitizer

    Winter Apple

    Kills 99.99% of germs

    2 fl oz (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    WINTER APPLE 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-119
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-119-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/24/2016
    2NDC:41250-119-1030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/24/2016
    3NDC:41250-119-0633 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/24/2016
    4NDC:41250-119-34237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/24/2016
    5NDC:41250-119-38296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/24/2016
    6NDC:41250-119-32355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/24/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/24/2016
    Labeler - Meijer Distribution, Inc (006959555)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(41250-119)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(41250-119)
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