Label: ANTIMICROBIAL WIPES WIPES- chlorhexidine and miconazole nitrate solution

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 7, 2022

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

  • ACTIVE INGREDIENTS

    Chlorhexidine Gluconate (2%)

    Miconazole Nitrate (2%)

  • PURPOSE

    ANTIBACTERIAL

    ANTIFUNGAL

  • INACTIVE INGREDIENT

    Purified Water, Propylene Glycol, Peg 5 cocamide, Benzyl Alcohol, and fragance.

  • WARNINGS AND PRECAUTIONS

    Warnings

    • For Animal Use Only
    • For topical use on dogs and cats.
    • Avoid contact with eyes and mucous membranes.
    • If eye contact occurs or skin irritation develops, rinse thoroughly with water, discotinue use and immediately consult your veterinarian.
  • DOSAGE & ADMINISTRATION

    Directions for use

    Apply to affected areas as directed by your veterinarian.

  • STORAGE AND HANDLING

    Storage: Store at room temperature ( 59 °F- 86 °F)

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Nootie_Antimicrobial Wipes 70 ct

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL WIPES  WIPES
    chlorhexidine and miconazole nitrate solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51437-205
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE3 mg  in 1 mL
    MICONAZOLE (UNII: 7NNO0D7S5M) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEG-5 COCAMINE (UNII: ZA36V5XS8F)  
    POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51437-205-6075 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2010
    Labeler - Nootie (008995795)