Label: EXPRESS WIPES HAND SANITIZER- hand sanitizer wipe liquid

  • NDC Code(s): 67858-645-01, 67858-645-02
  • Packager: QuestSpecialty Corporation
  • 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 June 4, 2020

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

View All Sections
  • label

    Product Label

    Active Ingredient Purpose

    Ethyl Alcohol 70%...... Antiseptic

    Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consulta a doctor.

    Do not use in the eyes.

    Flammable. Keep awaay from fire or flame.

    For external use only.

    Keep out of reah of children. If swallowed, get medical help or contact a Poison Cotnrol Center righ away.

    • Store below 110 oF (43 oC).

    Water, Propylene Glycol, Undeceth-7, Isopropyl Myristate, Aloe Barbacdensis Leaf Juice, Methyl Salicylae, Tocophenyl Aceate (Vitamin E).

    • For handwashing to decrease bacterial on the skin.
    • After changing diapers.
    • After assisting ill persons.
    • Before contact with a person under medical care or treatment.
    • Recommended for repeat use.

    • Wet hands thoroughly with product and allow to dry.,
    • Children under six years of age shoudl be supervised when using this product.

    Antiseptic

  • INGREDIENTS AND APPEARANCE
    EXPRESS WIPES HAND SANITIZER 
    hand sanitizer wipe liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67858-645
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL7 g  in 10 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67858-645-026 in 1 CARTON06/04/2020
    1NDC:67858-645-01210 g in 1 CANISTER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/04/2018
    Labeler - QuestSpecialty Corporation (103840377)
    Establishment
    NameAddressID/FEIBusiness Operations
    QuestSpecialty Corporation103840377manufacture(67858-645)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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