SANNYTIZE HAND SANITIZER (ALCOHOL) GEL [DYNAREX CORPORATION]

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SANNYTIZE HAND SANITIZER (ALCOHOL) GEL [DYNAREX CORPORATION]
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NDC 67777-317-01, 67777-317-02, 67777-317-03, 67777-317-04, 67777-317-05, 67777-317-06, 67777-317-07
Set ID 2aa8cd78-1e3f-4c39-8ebc-049bd8dcc6f2
Category HUMAN OTC DRUG LABEL
Packager Dynarex Corporation
Generic Name
Product Class
Product Number
Application Number PART333A
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  • ACTIVE INGREDIENT

    Active Ingredient                         Purpose

    Ethyl Alcohol 0.62%                   Antiseptic Handwash

  • WARNINGS

    • For external use only
    • Flammable, keep away from fire and flame
    • Do not use in or near the eyes
    • 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 andredness develops
  • PURPOSE

    An antiseptic handwash.

  • INDICATIONS & USAGE

    Cleaning and antiseptic cleansing of hands and skin.

  • 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, Carbomer, Triethanolamine, Aloe barbadensis juice, Fragrance

  • Label

    1432 IN GVIN010

  • INGREDIENTS AND APPEARANCE
    SANNYTIZE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-317
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-317-0129.5 mL in 1 BOTTLE; Type 0: Not a Combination Product04/25/2017
    2NDC:67777-317-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product04/25/2017
    3NDC:67777-317-03118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/25/2017
    4NDC:67777-317-04236 mL in 1 BOTTLE; Type 0: Not a Combination Product04/25/2017
    5NDC:67777-317-05473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/25/2017
    6NDC:67777-317-061.035 mL in 1 PACKET; Type 0: Not a Combination Product04/25/2017
    7NDC:67777-317-071.035 mL in 1 PACKET; Type 0: Not a Combination Product04/25/2017
    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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