Label: ARAMARK HAND SANITIZER- alcohol gel

  • 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 May 20, 2021

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

  • Active Ingredient

    Ethyl Alcohol 66.5%

  • Purpose

    Antibacterial

  • Uses

    ■ for hand washing to decrease bacteria on skin without soap and water

    ■ recommended for repeated use

  • Warnings

    For external use only.

    Flammable., keep away from fire or flame.

    Do not use in eyes.

    If this happens, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation and redness develop and persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    ■ wet hands and wrists thoroughly with product and allow to dry without wiping

    ■ children under 6 years of age should be supervised while using this product

  • Inactive Ingredients

    aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified

    water, triethanolamine

  • Package Labeling

    aramark

    25 ct.  Each Packet Net. Wt. 0.9g

    ​HAND SANITIZER

    Kills 99.9% of Germs

    Enriched with Aloe Vera

    NDC 81238-1112-2

    aramarkuniform.com

    MANUFACTURED FOR:

    Aramark

    Lenexa, KS 66219

    (913) 269-9611

    Please retain carton for drug information.

    1112-2 25ct Box

    1112-2 Packet

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  • INGREDIENTS AND APPEARANCE
    ARAMARK HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81238-1112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL66.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE (UNII: V5VD430YW9)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81238-1112-225 in 1 BOX05/21/2021
    10.9 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/21/2021
    Labeler - Western First Aid Safety DBA Aramark (043861524)
    Registrant - Western First Aid Safety DBA Aramark (043861524)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc.874965262manufacture(81238-1112)