Label: MICRELL ANTIBACTERIAL LTN SP- chloroxylenol liquid

  • NDC Code(s): 21749-975-04, 21749-975-08, 21749-975-10, 21749-975-12, view more
    21749-975-20, 21749-975-33, 21749-975-37, 21749-975-50, 21749-975-52, 21749-975-80
  • Packager: GOJO INDUSTRIES, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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

View All Sections
  • Active ingredient

    Chloroxylenol 0.3%

  • Purpose

    Antimicrobial

  • Use

    • Handwash to help decrease 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 with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

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

  • Directions

    • Wet hands

    • Apply a small amount of product and work into a lather

    • Rinse well and dry hands completely

  • Inactive ingredients

    Water (Aqua), Coconut Acid, Oleic Acid, Sodium Sulfate, Ethanolamine, Cocamide MEA, Coco-Betaine, Propylene Glycol, Retinyl Palmitate, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Hydroxypropyl Methylcellulose, Fragrance (Parfum)

  • PRINCIPAL DISPLAY PANEL

    Package LabelPackage LabelPackage LabelPackage LabelPackage Label

    Package Label
  • INGREDIENTS AND APPEARANCE
    MICRELL ANTIBACTERIAL LTN SP 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-975
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Chloroxylenol (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) Chloroxylenol0.003 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Coconut Acid (UNII: 40U37V505D)  
    Oleic Acid (UNII: 2UMI9U37CP)  
    Sodium Sulfate (UNII: 0YPR65R21J)  
    MONOETHANOLAMINE (UNII: 5KV86114PT)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    Coco-Betaine (UNII: 03DH2IZ3FY)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CORN OIL (UNII: 8470G57WFM)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-975-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    2NDC:21749-975-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    3NDC:21749-975-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    4NDC:21749-975-50500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    5NDC:21749-975-80800 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    6NDC:21749-975-101000 mL in 1 BAG; Type 0: Not a Combination Product07/30/1998
    7NDC:21749-975-331000 mL in 1 PACKAGE; Type 0: Not a Combination Product07/30/1998
    8NDC:21749-975-202000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    9NDC:21749-975-373784 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/1998
    10NDC:21749-975-52196841 mL in 1 DRUM; Type 0: Not a Combination Product07/30/1998
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/30/1998
    Labeler - GOJO INDUSTRIES, INC. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-975)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414label(21749-975) , pack(21749-975)
    Establishment
    NameAddressID/FEIBusiness Operations
    Travis Association for the Blind026032268label(21749-975) , pack(21749-975)
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!