Label: SANNYTIZE HAND SANITIZER WIPE- alcohol gel

  • NDC Code(s): 67777-320-01, 67777-320-02
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL

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 29, 2022

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  • ACTIVE INGREDIENT

    Active Ingredient                         Purpose

    Ethyl Alcohol 70%                   Antiseptic Wipe

  • WARNINGS

    • For external use only
    • Flammable, keep away from fire and flame
    • When using this product avoid contact with eyes. In case of eye contact, rinse with water to remove.
    • Stop use and ask a doctor if irritation and redness develops
  • PURPOSE

    Antiseptic handwash

  • INDICATIONS & USAGE

    For hand washing to decrease bacteria on the skin. Recommended for repeated use.

  • DOSAGE & ADMINISTRATION

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

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN, if swallowed get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENTS

    Inactive ingredients: Water, Glycerin, Propylene glycol, Diazolidinyl urea, Aloe barbadensis leaf juice, Polysorbate 20, Carbomer, Tocopherol acetate, Methylparaben, Propylparaben, Triethanolamine

  • PRINCIPAL DISPLAY PANEL

    1306 IN MasterDynarex SannyTizer HandSanitizing Wipes

    Sannywipe.jpg

  • INGREDIENTS AND APPEARANCE
    SANNYTIZE HAND SANITIZER WIPE 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-320
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-320-021620 in 1 CASE04/25/2017
    1NDC:67777-320-01135 in 1 CANISTER
    13.42 mL in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/25/2017
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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