Ear Dry

Manufacturer
Cardinal Health | Product Quest Mfg
Effective date
2018-08-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:52:57

Label at a glance#

ProductEar Dry Leader
Active ingredientIsopropyl Alcohol
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 94.998%, Glycerin 5.0%

INDICATIONS & USAGE SECTION

Uses

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

WARNINGS SECTION

Warnings

Do not use: if you have ear drainage or discharge, ear pain, irritation or rash in the ear, or are dizzy; consult a doctor.  If you have an injury or perforation (hole) of the ear drum of after ear surgery unless directed by a doctor.  Avoid contact with eyes.  If accidental contact occurs, flush eyes with water and consult a doctor. Discontinue use and consult a doctor if:  undue irritation or sensitivity occurs.

DOSAGE & ADMINISTRATION SECTION

Directions

FOR USE IN THE EAR ONLY.  To use:  remove cap, apply 4-5 drops in each ear after exposing ears to water such as swimming, showering or bathing or as directed by a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aloe Barbadensis Leaf Juice, Chamomile Recutita (Matricaria) Flower Oil.

OTC - PURPOSE SECTION

Purpose

Helps dry and relieve water-clogged ears.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37205-619-012025-04-29C16284748780-19d75b9d0-3706-f424-e053-dadaa90a57ceDrug Facts
37205-619-012020-01-31C16284748780-19d75b9d0-3706-f424-e053-dadaa90a57ceDrug Facts

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37205-61937205-619-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
76e26afd-1203-4e8e-9595-643315a26f8753cd5182-c697-4833-a88e-b443c9f4b0262025-04-24WarningsExact identifier
spl set id: 53cd5182-c697-4833-a88e-b443c9f4b026

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.