Label: LFG- chloroxylenol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 9, 2022

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

  • Drug Facts

  • Active Ingredient

    CHLOROXYLENOL 0.3%

    Purpose

    Antimicrobical

  • Uses

    For hand washing to decrease bacteria on skin

  • Warnings

    For external use only 

    When using this product

    avoid contact with eyes. In case of contact flush with water.

    Keep out of reach of children.

    except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Wet hands. Apply small amount to hands. Scrub thoroughly. Rinse. For children under 6 use only under adult supervision.

  • Inactive Ingredients

    Water, Sodium Laureth Sulfate, Cocamide Methyl Mea, Cocamidopropyl Betaine, Glycerin, Sodium Citrate, Sodium Chloride, Tocopherol, Fragrance, Citric Acid, Alcohol, Methylisothiazolinone, Methylchloroise thiazolinone, Magnesium Chloride, Magnesium Nitrate, Disodium Edita.

  • Package Labeling:

    Box

  • INGREDIENTS AND APPEARANCE
    LFG 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77879-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77879-006-00473 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/15/2020
    Labeler - BT Supplies West Inc (033878488)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang iColor Biotech Co., Ltd554528308manufacture(77879-006)