Label: SIMPLIFY ANTIBACTERIAL HAND WIPES FRESH SCENT- benzalkonium chloride cloth

  • NDC Code(s): 11822-0284-1, 11822-0285-1
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 29, 2024

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

View All Sections
  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium chloride 0.13%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses

    • to decrease bacteria on the skin
    • recommended for repeated use
  • WARNINGS

    Warnings

    For external use only

    When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

    Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions

    • rub wipe thoroughly over all surfaces of both hands
    • allow to dry without wiping
    • supervise children under 6 years old
    • not recommended for infants
    • dispose of wipe in trash, do not flush
  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Alcohol Denat., Phenoxyethanol, PEG-8 Dimethicone, Caprylyl Glycol, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Potassium Sorbate, Disodium EDTA, Citric Acid, Fragrance, Aloe Barbadensis Leaf Juice

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY: RITE AID,

    200 NEWBERRY COMMONS

    ETTERS, PA 17319

    www.riteaid.com

    MADE IN CHINA

  • PDP 11822-0284

    Simplify ®

    Antibacterial

    Hand Wipes

    FRESH SCENT

    Kills 99.9% of Germs

    With Moisturizing Aloe

    Gentle on skin

    Hypoallergenic

    DO NOT FLUSH

    24 Wipes

    Individually Wrapped

    5.0 IN x 7.8 IN

    (12.7 cm x 19.8 cm)

    box label

  • PDP 11822-0285

    Simplify®

    Antibacterial

    Hand Wipes

    FRESH SCENT

    Kills 99.9% of Germs

    With Moisturizing Aloe

    Gentle on skin

    Hypoallergenic

    DO NOT FLUSH

    40 Wipes

    5.7 IN x 7.5 IN

    (14.5 cm x 19.05 cm)

    label

  • INGREDIENTS AND APPEARANCE
    SIMPLIFY ANTIBACTERIAL HAND WIPES  FRESH SCENT
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0284
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0284-124 in 1 BOX07/23/2024
    11 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/23/2024
    SIMPLIFY ANTIBACTERIAL HAND WIPES  FRESH SCENT
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0285
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0285-140 in 1 CONTAINER; Type 0: Not a Combination Product07/23/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/23/2024
    Labeler - Rite Aid Corporation (014578892)
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!