Label: RAYON BAMBOO HEAVY DUTY ANTISEPTIC HAND SANITIZER WIPES- benzalkonium chloride cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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

View All Sections
  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antiseptic

  • Use

    For handwashing to decrease bacteria on the skin.

  • Warnings

    For external use only

    Do not use

    in the eyes

    Stop use and ask a doctor if

    • irritation and redness develop.
    • if condition persists for more than 72 hours consult a doctor.

    Keep out of reach of children.

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

  • Directions

    • Peel back the foil seal and pull the center wipe through the slot in the lid.
    • Wet hands thoroughly with product and allow to dry without wiping.
    • Close lid after use to prevent wipes from drying out.
  • Inactive ingredients

    Water, Estol, Poloxalene, PEG-75 Lanolin, Glycerin, Aloe Barbadensis Extract, Polyethylene glycol, Lauryl glycoide, Fragrance, Disodium EDTA, -Bromo-2-Nitropropane-1,3-Diol, 1,2-Benzisothiazolin-3-One

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    RAYON BAMBOO HEAVY DUTY ANTISEPTIC HAND SANITIZER WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90119-002
    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
    BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)  
    WATER (UNII: 059QF0KO0R)  
    POLOXALENE (UNII: V8B3K56SW0)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    BRONOPOL (UNII: 6PU1E16C9W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90119-002-2525 in 1 PACKAGE01/05/2021
    17.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/05/2021
    Labeler - Orbizorb LLC (117447551)
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!