Label: SUAVE- ethyl alcohol liquid liquid

  • 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 December 7, 2022

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

View All Sections
  • SUAVE HAND SANITIZER SPRAY - Ethyl Alcohol liquid

    Suave Hand Sanitizer Spray

  • Drug Facts

    Active ingredient

    Ethyl Alcohol (65%)

  • Purpose

    Antiseptic

  • Uses

    help decrease bacteria on the hands

  • Warnings

    • For external use only
    • Flammable. Keep away from fire or flame
    • Avoid contact with eyes,     in case of contact, rinse eyes thoroughly with water immediately.
    • If irritation develps, discontinue use and consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children except under adult supervision.
    If swallowed, get medical help or contact a poison control Center right away.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping. Rub lightly until dry. Do not rinse.

  • Other information

    May discolor fabrics or surfaces. Store below 105˚F (40˚C).

  • Inactive ingredients

    Glycerin, Water (Aqua).

  • Questions?

    Call us at 1-800-782-8301.

  • Packaging

    DoveHandSanitizerSpray

  • INGREDIENTS AND APPEARANCE
    SUAVE 
    ethyl alcohol liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1735
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL650 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1735-1295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/20/2020
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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!