Ear Wax Removing Drops

Manufacturer
Cardinal Health
Effective date
2012-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:49:41

Label at a glance#

ProductEar Wax Removing Drops Carbamide Peroxide
Active ingredientCarbamide Peroxide
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Carbamide Peroxide 6.5%

OTC - PURPOSE SECTION

Purpose

Carbamide Peroxide 6.5%

INDICATIONS & USAGE SECTION

Uses

For occasional use as an aid to soften, loosen, and remove excessive ear wax.

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 eardrum or after ear surgery, unless directed by a doctor.  For more than four consecutive days.

When using this product: avoid contact with the eyes.

Stop use and ask a doctor if: excessive ear wax remains after use of this product for four consecutive days.

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.  If accidental contact with eyes occurs, flush eyes with water and consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Directions

FOR USE IN THE EAR ONLY.  Adults and children over 12 years of age:  tilt head sideways and place 5 to 10 drops into ear.  Tip of applicator should not enter ear canal.  Keep drops in ear for several minutes by keeping head tilted or placing cotton in ear.  Use twice daily for up to four days if needed, or as directed by a doctor.  Any wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe.  Children under 12 years of age:  consult a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Glycerin, Oxyquinoline, Aloe Barbadensis Leaf Extract, Anthemis Nobilis Flower Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ear Wax Cleansing Kit

Step 1 Ear Wax Removing Drops

Step 2 Ear Cleansing Spray

bottle imagebottle imagecarton imagecarton image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37205-615-562025-04-22C16284748780-19d75b9d0-f8cb-f424-e053-dadaa90a57ceDrug Facts
37205-615-562020-01-31C16284748780-19d75b9d0-f8cb-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Carbamide PeroxideACTIVE INGREDIENT31PZ2VAU811
Carbamide PeroxideACTIVE MOIETY31PZ2VAU811
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X1
CHAMAEMELUM NOBILE FLOWER OILINACTIVE INGREDIENTUB275878391

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37205-61537205-615-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

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
faf79d2a-fede-4408-b31a-ccfe13fde47f1a1523f0-9d65-44de-afab-a0df6faebb8a2025-04-16WarningsExact identifier
spl set id: 1a1523f0-9d65-44de-afab-a0df6faebb8a

Reported adverse events (FAERS/openFDA)#

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