Instant Ear Dry

Manufacturer
WalMart | Product Quest
Effective date
2018-01-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:53:55

Label at a glance#

ProductInstant Ear Dry Equate
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

Active ingredient                         Purpose

OTC - ACTIVE INGREDIENT SECTION

ISOPROPYL ALCOHOL             95.0%

INDICATIONS & USAGE SECTION

Uses
Dries water in the ears and relieves water-clogged ears, thereby relieving discomfort, the sensation of fullness or hearing impairment

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame

Do not use • in the eyes

Ask doctor before use if you have • ear drainage or discharge • ear pain • irritation or rash in ear • dizziness •  recently had ear surgery

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children
If product is swallowed, get medical help or contact a Poison Control Center right away
In case of accidental ingestion, seek professional or contact a Poison Control Center immediately.

Direction

DOSAGE & ADMINISTRATION SECTION

Apply 4-5 drops in each affected ear

Inactive ingredient

INACTIVE INGREDIENT SECTION

ISOPROPYL ALCOHOL, GLYCERIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-033-012020-01-31C16284748780-19d75b9d0-9c22-f424-e053-dadaa90a57ce315355aa-2fe8-4ddb-bc35-729aabec4427

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-03349035-033-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
61cbd778-48a1-d8b4-e053-2a91aa0a1bfe315355aa-2fe8-4ddb-bc35-729aabec44272018-01-02WarningsExact identifier
spl id: 61cbd778-48a1-d8b4-e053-2a91aa0a1bfe
spl set id: 315355aa-2fe8-4ddb-bc35-729aabec4427

Reported adverse events (FAERS/openFDA)#

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