Label: MAXSAVER SANITIZING WIPES- benzalkonium chloride cloth

  • NDC Code(s): 71293-021-01, 71293-021-02, 71293-021-03, 71293-021-04
  • Packager: ERC ACQUISITION, INC.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 26, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13 %

  • Purpose

    Antimicrobal

  • Use

    Hand sanitizer to help reduce bacteria on the skin.

    Recommended for repeated use.

  • Warnings

    For external use only.

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

    Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

    If swallowed get medical help or contact a poison control center immediately.

    Keep out of reach of children.

  • Directions

    • Wet hands thoroughly with product and allow to dry.
    • Be sure to use entire wipe.
    • Discard after single use.
    • Children under 6 years of age should be supervised when using this product.
  • Inactive ingredients

    Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, Water

  • PRINCIPAL DISPLAY PANEL

    MaxSaver™

    Sanitizing Wipes

    Kills 99.99%

    of most common germs that

    may cause illness

    DO NOT

    FLUSH

    ERC

    Fragrance Free

    ercwipe.com

    ERC WIPING PRODUCTS

    2000 Wipes • 8"x 5"

    800-225-9473

    undefined

  • INGREDIENTS AND APPEARANCE
    MAXSAVER  SANITIZING WIPES
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71293-021
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71293-021-026 in 1 BOX07/18/2023
    1NDC:71293-021-012000 in 1 CANISTER; Type 0: Not a Combination Product
    2NDC:71293-021-044 in 1 BOX07/18/2023
    2NDC:71293-021-032000 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/18/2023
    Labeler - ERC ACQUISITION, INC. (019312339)
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

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!