Label: EAR DRY DROPS WELL AT WALGREENS- isopropyl alcohol 94.998% glycerin 5% liquid

  • 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 January 30, 2018

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

View All Sections
  • Active ingredients                     

    Isopropyl Alcohol 94.998%         

    Glycerin 5.0%                              

  • Purpose

    Helps dry and relieve water-clogged ears

  • Uses

    Helps relieve the discomfort of water-clogged ears by drying excess water due to water activities.

  • Warnings

    Flammable: ​Keep away from fire or flame

  • Do not use • in the eyes

  • Ask doctor before use if you have

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

    • irritation or pain occurs
  • Keep out of reach of the children

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

  • Directions

    Apply 4 to 5 drops in each affected ear

  • Inactive ingredient

    Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    EAR DRY DROPS  WELL AT WALGREENS
    isopropyl alcohol 94.998% glycerin 5% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-3019
    Route of AdministrationAURICULAR (OTIC)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl Alcohol (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) Isopropyl Alcohol94.998   in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    Glycerin (UNII: PDC6A3C0OX) 5.0 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-3019-011 in 1 CARTON04/15/2013
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34404/15/2013
    Labeler - Walgreens (008965063)
    Registrant - Product Quest Mfg (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg927768135manufacture(0363-3019) , label(0363-3019)
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!