Label: HYGIENE CLEAN LUXURY CLEAN HAND SANITIZER ON THE GO AND CAR SAFE- benzalkonium chloride liquid

  • NDC Code(s): 80499-031-01, 80499-031-02, 80499-031-03, 80499-031-04
  • Packager: USA Broom LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 28, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antimicrobial

  • Uses

    - For hand sanitizing to decrease the bacteria on skin.

    - Recommended for repeated use.

  • Warnings

    For external use only.

    When using this product

    avoid contact with eyes. In case of eye contact, flush eyes with water

    Stop use and ask a doctor if

    irritation or redness develops, or if condition persists for more than 72 hours.

    KEEP OUT OF REACH OF CHILDREN.

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

  • DIRECTIONS

    -Pump a small amount of foam into palm of hand

    -Rub thoroughly over all surfaces of both hands

    -Rub hands together briskly until dry

  • Inactive ingredients:

    Water; Propylene Glycol; Lauramine Oxide; Undeceth-7; DisodiumEDTA; Aloe Barbadensis Gel; Glycereth-2-Cocoate; DMDM Hydantoin; Fragrance; Citric Acid

  • Package Labeling:50ml

    Bottle3

  • Package Labeling:237ml

    Bottle4

  • Package Labeling:50ml (24 Bottles)

    Bottle5

  • Package Labeling:237ml (24 Bottles)

    Bottle6

  • INGREDIENTS AND APPEARANCE
    HYGIENE CLEAN LUXURY CLEAN HAND SANITIZER ON THE GO AND CAR SAFE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80499-031
    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
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    UNDECETH-7 (UNII: R6B5PCO2JN)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80499-031-0150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/28/2021
    2NDC:80499-031-02237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/28/2021
    3NDC:80499-031-0324 in 1 BOX02/28/2021
    350 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:80499-031-0424 in 1 BOX02/28/2021
    4237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/28/2021
    Labeler - USA Broom LLC (117638854)
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!