Label: SANNYTIZE HAND SANITIZER- hand sanitizer gel

  • NDC Code(s): 67777-010-01, 67777-010-02, 67777-010-03, 67777-010-04, view more
    67777-010-05, 67777-010-06, 67777-010-10, 67777-010-11, 67777-010-12, 67777-010-13, 67777-010-14, 67777-010-15, 67777-010-16, 67777-010-17, 67777-010-18, 67777-010-19, 67777-010-20
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic Handwash

  • Use

    • For hand washing to decrease bacteria on the skin.
  • Warnings

    For External Use Only

    Flammable. Keep away from fire or flame

    Do not use

    In 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 and redness develop.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping
  • Other Information

    • Do not store above 110°F (43ºC)
    • May discolor some fabrics
    • Recommended for repeated use
  • Inactive Ingredients

    Aloe Vera Leaf Extract, Carbopol Ultrez 10, Fragrance, Glycerin, Propylene Glycol, Purified Water,Triethanolamine

  • Questions?

    1-888-396-2739 Monday - Friday, 9AM - 5PM EST

  • Label

    1428-BX-GVIN0101428 Hand Sanitizer

  • Label

    1427 Hand Sanitizer

  • Label

    1427-BX-GVIN0101427 Hand Sanitizer

  • Label

    1429-BX-GVIN0101429 Hand Sanitizer

  • Label

    1431- GVIN0101431 Hand Sanitizer

  • Label

    1432-GVIN0101432 Hand Sanitizer

  • Label

    1433-GVIN0101433 Hand Sanitizer

  • Label

    1427-BX-MASTER1427 Hand Sanitizer

  • Label

    1428-BX-MASTER1428 Hand Sanitizer

  • Label

    1429-BX-MASTER1429 Hand Sanitizer

  • Label

    1431-IN-MASTER1431 Hand Sabitizer

  • Labels

    1432-IN-MASTER1432 Hand Sanitizer

  • Label

    1433-BX-MASTER1433 Hand Sanitizer

  • Label 1433UB-10

    1433UB-10_BX_MASTER1433UB-10

  • INGREDIENTS AND APPEARANCE
    SANNYTIZE HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-010-01144 in 1 CASE11/01/2019
    1NDC:67777-010-1124 in 1 BOX
    1NDC:67777-010-1029.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:67777-010-02144 in 1 CASE11/01/2019
    2NDC:67777-010-1324 in 1 BOX
    2NDC:67777-010-1259 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:67777-010-0396 in 1 CASE11/01/2019
    3NDC:67777-010-1524 in 1 BOX
    3NDC:67777-010-14118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:67777-010-0448 in 1 CASE11/01/2019
    4NDC:67777-010-16236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:67777-010-0512 in 1 CASE11/01/2019
    5NDC:67777-010-17473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    6NDC:67777-010-061728 in 1 CASE11/01/2019
    6NDC:67777-010-18144 in 1 BOX
    61.01 mL in 1 PACKET; Type 0: Not a Combination Product
    7NDC:67777-010-201000 in 1 CASE11/01/2019
    7NDC:67777-010-1910 in 1 BOX
    71.01 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/01/2019
    Labeler - Dynarex Corporation (008124539)
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