Label: HAND SANITIZING WIPES- ethyl alcohol cloth

  • NDC Code(s): 60913-415-11
  • Packager: PHOENIX HEALTHCARE SOLUTIONS, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

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

  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 62% v/v

  • Purpose

    Antimicrobial

  • Uses

    Hand sanitizer to help reduce bacteria on the 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.

    Discontinue use and ask a doctor if

    ■ Irritation or rash appears and lasts.

    Keep out of reach of Children

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

  • Directions

    Unfold towelette; Wipe hands; Discard after use

  • Inactive ingredient

    Purified Water

  • Other information

    ■  Store at room temperature: 15℃~30℃(59℉~86℉)
    ■  May discolor certain fabrics or surfaces

  • Questions

    +1-954-607-6080

  • Other Information

    KILLS 99.99% OF GERMS*

    Single Use Only

    Do Not Flush

  • Principal Display Panel

    NDC 60913-415-11

    Alcohol Formula, Fragrance Free, Paraben Free

    Phoenix Healthcare Solutions, LLC

    "An Innovative Medical Manufacturer"

    HAND SANITIZING WIPES

    KILLS 99.99% OF GERMS*

    5.1 in. X 5.9 in. (13 cm X 15 cm)

    110 INDIVIDUALLY WRAPPED WIPES

    Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZING WIPES 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60913-415
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60913-415-11110 in 1 BOX08/06/2019
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/06/2019
    Labeler - PHOENIX HEALTHCARE SOLUTIONS, LLC (079146847)
    Registrant - PHOENIX HEALTHCARE SOLUTIONS, LLC (079146847)
    Establishment
    NameAddressID/FEIBusiness Operations
    Phoenix Innovative Healthcare Manufacturers Private Limited650743854manufacture(60913-415)