Label: ZEP ACCLAIM AB- benzalkonium chloride liquid

  • NDC Code(s): 66949-131-01, 66949-131-11, 66949-131-16
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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

View All Sections
  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antiseptic Hand Wash

  • Uses

    Hand washing to decrease bacteria on skin.

  • Warnings

    For external use only.

  • Do not use

    Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

  • When using this product

    • Do not swallow.
    • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
  • Stop use and ask a doctor

    Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

  • Keep out of reach of children

    Keep out of reach of children except under adult supervision.

  • Directions

    • Wet hands with water.
    • Place hands under dispenser and apply liquid soap.
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.
  • Other Information

    • Store at room temperature.
    • Do not freeze.
    • Dispose in accordance with all applicable federal, state, and local regulations.
  • Inactive Ingredients

    Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Cocamide DIPA, PEG-120 Methyl Glucose Dioleate, Sodium Chloride, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Fragrance, Yellow 5, Red 4

  • Questions or comments?

    Call 1-877-BUY-ZEP (1-877-428-9937)

  • PRINCIPAL DISPLAY PANEL

    131_3149

  • INGREDIENTS AND APPEARANCE
    ZEP ACCLAIM AB 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-131
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
    COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-131-0111400 mL in 1 CASE; Type 0: Not a Combination Product12/15/2016
    2NDC:66949-131-166000 mL in 1 CASE; Type 0: Not a Combination Product12/15/2016
    3NDC:66949-131-116000 mL in 1 CASE; Type 0: Not a Combination Product12/15/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/15/2016
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-131)
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!