Label: NASOVA EAR DRYING DROPS- isopropyl alcohol 95% solution/ drops

  • NDC Code(s): 57483-350-15
  • Packager: Innovus Pharmaceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 December 31, 2022

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active ingredients

    Isopropyl alcohol 95% in an anhydrous glycerin base

  • Purpose

    Ear drying aid

  • Uses

    Dries water in the ears and relieves water-clogged ears

  • Warnings

    Flammable: Keep away form fire or flame

  • Do not use

    in the eyes

  • Aslk a doctor before use if you have

    • ear drainage or discharge
    • pain, irritation, or rash in the ear
    • have had ear surgery
    • dizziness
  • Stop use and ask a doctor if

    Irritation (too much burning) or pain occurs

  • Keep out of reach of children 

    In case of accidental ingestion, seek professional assistant or contact a Poison Control Center immediately.

  • Directions

    • Apply 4 to 5 drops in each affected ear
  • Other Information 

    • Store at room temperature
    • Keep tightly closed
  • Inactive ingredients

    Glycerin

  • Questions?

    Call 1.800.996.5122 (Mon-Fri 9AM-5PM EST)

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    NASOVA EAR DRYING DROPS 
    isopropyl alcohol 95% solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57483-350
    Route of AdministrationAURICULAR (OTIC)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL950 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57483-350-152 in 1 CARTON11/02/2021
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34411/02/2021
    Labeler - Innovus Pharmaceuticals, Inc. (962507187)
    Establishment
    NameAddressID/FEIBusiness Operations
    AMMAN PHARMACEUTICAL INDUSTRIES534677849manufacture(57483-350)
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

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!