Label: VIDA MIA HAND SANITIZER (62%)- alcohol gel

  • 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 December 23, 2014

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  • Drug Facts

    Active Ingredient

    Ethyl Alcohol 62%

    Purpose

    Antibacterial

  • Uses

    • Decreases bacteria on skin.
  • Warnings

    For external use only.

    Flammable. Keep away from heat or flame.

  • DOSAGE & ADMINISTRATION

    When using this product, avoid contact with eyes. In case of contact flush eyes with water.

    Stop use and ask a doctor if redness or irritation develops & persists for more than 72 hours.

  • Keep out of the reach of children.

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

  • Directions

    • Wet hands thoroughly with product and allow to dry.
    • Children under 6 years of age, use only under adult supervision.
  • Other Information

    • Do not store above 105° F (43°C).
    • May discolor some fabrics and surfaces.
  • Inactive Ingredients

    AQUA, CARBOMER, DIISOPROPYLAMINE, POLYSORBATE 80, CETYL ACETATE, ACETYLATED LANOLIN ALCOHOL, PROPYLENE GLYCOL, DIAZOLINYL UREA, METHYLPARABEN, PROPYLPARABEN, FRAGRANCE.

  • SPL UNCLASSIFIED SECTION

    Dial is a registered trademark of Pure & Natural Company.

  • Distributed by/ Distribuido por

    Magellan Distribution Solutions

    Medley, Florida 33178

  • Vida Miami salud

    Compare to/ Compare con Dial Hand Sanitizer

    HAND SANITIZER

    DESINFECTANTE DE MANOS


    Kills 99.9% of Germs

    Moisturizes & Conditions the Skin

    Mata 99.9% de Germenes

    Hidrata & Acondiciona la Piel

    16 FL OZ (453ml)

    59970-170-16

    image description

  • INGREDIENTS AND APPEARANCE
    VIDA MIA HAND SANITIZER  (62%)
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59970-170
    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
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    CETYL ACETATE (UNII: 4Q43814HXS)  
    ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59970-170-16453 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/20/2014
    Labeler - Navarro Discount Pharmacies,LLC (094930963)
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