Label: 7 ELEVEN HAND SANITIZER MOUNTAIN SPRING SCENT- ethanol gel

  • 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 September 19, 2022

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredient Purpose

    Ethanol 70% v/v........Antiseptic

  • WARNINGS

    Warnings

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

  • WHEN USING

    When using this product

    Avoid contact with eyes. In case of eye contacy, flush eyes with water.

    Stop use and ask a doctor if irritaiton or redness develops and conditions persist for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

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

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water, Glycerin, Polyacrylic Acid, Frangrance, Dye.

  • PURPOSE

    Antiseptic, Hand Sanitizer

  • STOP USE

    Stop use and ask a doctor if irritation or redness develops and conditions persist for more than 72 hours.

  • INDICATIONS & USAGE

    Uses: For hand sanitizing to decrease bacteria on the skin.

  • DOSAGE & ADMINISTRATION

    Directions

    Place enough product in your palm to thoroughly cover hands. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

  • PRINCIPAL DISPLAY PANEL

    64 oz label64 ounce 81122-139-16

  • PRINCIPAL DISPLAY PANEL

    1.25 L Front Label1.25 Liters 81122-139-25

  • PRINCIPAL DISPLAY PANEL

    1.25 L Back Label1.25 Liters 81122139-25 Back Label

  • PRINCIPAL DISPLAY PANEL

    330 G 81122-139-33330 G 81122-139-33

  • INGREDIENTS AND APPEARANCE
    7 ELEVEN HAND SANITIZER MOUNTAIN SPRING SCENT 
    ethanol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81122-139
    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
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER (UNII: NX76LV5T8J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81122-139-6418900 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/16/2020
    2NDC:81122-139-25125000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product12/16/2020
    3NDC:81122-139-331249000 mL in 1 CONTAINER; Type 0: Not a Combination Product09/03/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/16/2020
    Labeler - Magnus Procurement & Logistics Solution, Inc. (012763630)
    Registrant - Seatex, LLC (026647404)
    Establishment
    NameAddressID/FEIBusiness Operations
    Seatex, LLC026647404manufacture(81122-139) , label(81122-139) , pack(81122-139)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!