Label: 2PK TRAVELER HAND SANITIZER LAVENDER- ethyl alcohol liquid

  • NDC Code(s): 52000-114-31
  • Packager: Universal Distribution Center LLC
  • 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 November 24, 2021

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 62.0%

  • Purpose

    Antimicrobial

  • Uses

    Hand Sanitizer to help reduce bacteria on skin.

  • WARNINGS

    Flammable. Keep away from fire or flame.
    For external use only.

    When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

    Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    • Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
    • Children under 6 years of age should be supervised when using this product.

  • Other Information:

    • Store below 106° F (41° C)
    • May discolor certain fabrics or surfaces.

  • INACTIVE INGREDIENTS:

    Water (Aqua) , Lavandula Angustifolia (Lavender) Flower Extract, Carbomer, Fragrance, Glycerin, Propylene Glycol, Triethanolamine, Tocopheryl Acetate, FD&C Blue No.1, D&C Red No.33.

  • SPL UNCLASSIFIED SECTION

    INSTANT HAND SANITIZER

    With Vitamin E & Other Moisturizers

    KILLS 99.9% OF BACTERIA

    Made in India

    Distributed by: Universal Distribution Center
    96 Distribution Boulevard • Edison, NJ 08817

  • Packaging

    52000-114

  • INGREDIENTS AND APPEARANCE
    2PK TRAVELER HAND SANITIZER LAVENDER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-114
    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)  
    LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-114-312 in 1 BLISTER PACK03/31/2020
    160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/31/2020
    Labeler - Universal Distribution Center LLC (019180459)