Label: ENT ESSENTIALS ALL DRY EAR DRYING DROPS- isopropyl alcohol liquid

  • NDC Code(s): 68093-4501-1
  • Packager: Wisconsin Pharmacal Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 November 28, 2017

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  • ACTIVE INGREDIENT

    Active Ingredients

    Isopropyl alcohol, 95%

  • PURPOSE

    Purpose

    Ear Drying aid in an Anhydrous glycerin base, 5%

  • INDICATIONS & USAGE

    Uses

    Dries water in the ears and relieves water-clogged ears after:

    • swimming
    • showering
    • bathing
    • washing the hair
  • WARNINGS

    Warnings

    Flammable:Keep away from fire or flame.

    Do not use in the eyes.

  • ASK DOCTOR

    Ask a doctor before use if you have

    • ear drainage or dischage
    • pain, irritiaon, or rash in ear
    • had ear surgery
    • dizziness
  • STOP USE

    Stop use and aks a doctor if irritation (too much burning) or pain occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep our of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    Apply 4 to 5 drops in each affected ear.

  • QUESTIONS

    Questions or comments?

    1-800-635-3696

  • INACTIVE INGREDIENT

  • PRINCIPAL DISPLAY PANEL

    Label and Carton

  • INGREDIENTS AND APPEARANCE
    ENT ESSENTIALS ALL DRY EAR DRYING DROPS 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68093-4501
    Route of AdministrationAURICULAR (OTIC)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.95 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68093-4501-11 in 1 CARTON02/01/2017
    133 g in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34402/01/2017
    Labeler - Wisconsin Pharmacal Company (800873986)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wisconsin Pharmacal Company800873986manufacture(68093-4501)
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