Label: ANTIMICROBIAL 652- chloroxylenol lotion

  • NDC Code(s): 54679-0001-1
  • Packager: Montgomery County Chapter Nysarc, Inc dba Liberty Enterprises
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 31, 2023

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

View All Sections
  • ACTIVE INGREDIENT:

    CHLOROXYLENOL

  • Purpose

    Antimicrobial

  • Uses

    Antimicrobial hand sanitizer.

  • INACTIVE INGREDIENTS:

    WATER, TALL OIL ACID, POTASSIUM HYDROXIDE, COCONUT ACID, PROPYLENE GLYCOL, SODIUM LAURYL SULFATE, COCAMIDE DEA, TETRASODIUM EDTA, SODIUM CHLORIDE, STYRENE/ACRYLATES COPOLYMER, FRAGRANCE, POLYMETHOXY BICYLIC OXAZOLIDINE, YELLOW 5.

  • DIRECTIONS:

    Dispense sufficient amount onto hands, add water, lather, and rinse.

  • WARNING:

    FOR EXTERNAL USE ONLY. Avoid contact witheyes. In case of eye contact, immediately flush with water. If eye or skin irritation persists, get medical advice/attention. If ingested, contact a physician or Poison Control Center immediately.

  • Keep out of reach of children.

    KEEP OUT OF REACH OF CHILDREN.

  • INACTIVE INGREDIENT

    Inactive ingredients - Water, Tall oil acid, Potasium hydroxide, Coconut acid, Propylene glycol,

    Sodium lauryl sulfate, Cocamide DEA, Tetrasodium EDTA, Sodium chloride, Styrene/Acrylates Copolymer,

    Fragrence, Polymethoxy biclic oxazolidine, Yellow 5.
    ​​​​​

  • ANTIMICROBIAL HAND LOTION SOAP product label

    ANTIMICROBIAL HAND LOTION SOAP #652 (NYSID # F6652)

    To order visit www.LibertyCleanProducts.com or contact NYS Industries for the Disabled at 800-221-5994. Packaged by: Liberty Enterprises, Amsterdam, NY 12010

    LOT NO.: 115 NET CONTENTS: 27 FL. OZ (800ML) Index: 01

    LibertyEnt 652 DPL

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL 652 
    chloroxylenol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54679-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3.6 mg  in 800 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TALL OIL ACID (UNII: H9HR63474M)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    COCONUT ACID (UNII: 40U37V505D)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)  
    5-HYDROXYMETHYL(METHYLENEOXY)-1-AZA-3,7-DIOXABICYCLO(3,3,0)OCTANE (UNII: 82EKS47IC5)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54679-0001-1800 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/1994
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/1994
    Labeler - Montgomery County Chapter Nysarc, Inc dba Liberty Enterprises (093257475)
    Registrant - Montgomery County Chapter Nysarc, Inc dba Liberty Enterprises (093257475)
    Establishment
    NameAddressID/FEIBusiness Operations
    Montgomery County Chapter Nysarc, Inc dba Liberty Enterprises093257475manufacture(54679-0001)
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!