Label: SUAVE- skin solutions hand sanitizer lotion lotion

  • 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 SKIN SOLUTIONS HAND SANITIZER LOTION - Benzalkonium Chloride lotion

    Suave Skin Solutions Hand Sanitizer Lotion

  • Drug Facts

    Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antiseptic

  • Uses

    helps decrease bacteria on the hands

  • Warnings

    For external use only
    Avoid contact with eyes,     In case of contact, rinse eyes thoroughly with water.
    If irritation develops, 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

    Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

  • Inactive ingredients

    Water (Aqua), Glycerin, Tapioca Starch, Polyquaternium-37, Dicaprylyl Carbonate, Phenoxyethanol, Caprylyl Glycol, Fragrance (Parfum), Lauryl Glucoside, Tocopheryl Acetate, Amyl Cinnamal, Benzyl Alcohol, Citronellol, Geraniol, Limonene, Linalool, Titanium Dioxide (CI 77891).

  • Call

    1-800-782-8301 or visit www.suave.com

  • Packaging

    Suave Hand Sanitizer Lotion

  • INGREDIENTS AND APPEARANCE
    SUAVE 
    skin solutions hand sanitizer lotion lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1850
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GERANIOL (UNII: L837108USY)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1850-188.5 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/01/2021
    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!