Auro Dri

Manufacturer
Insight Pharmaceuticals LLC
Effective date
2026-09-21
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-09-24 01:01:38

Label at a glance#

ProductAuro Dri
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Dosage and administration

unscrew cap from bottle remove foil safety seal from bottle affix applicator cap to bottle remove red applicator cap tip apply 4 to 5 drops in each affected ear

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

AURO-DRI®

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 95% in an anhydrous glycerin 5% base

Purpose

OTC - PURPOSE SECTION

Ear drying aid

Use

INDICATIONS & USAGE SECTION

dries water in the ears and relieves water-clogged ears after

  • swimming
  • showering
  • bathing
  • washing the hair

Warnings

WARNINGS SECTION

Flammable

Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

in the eyes

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • ear drainage or discharge
  • pain, irritation or rash in the ear
  • had ear surgery
  • dizziness

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation (too much burning) or pain occurs

Keep out ofreach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • unscrew cap from bottle
  • remove foil safety seal from bottle
  • affix applicator cap to bottle
  • remove red applicator cap tip
  • apply 4 to 5 drops in each affected ear

Other information 

OTHER SAFETY INFORMATION

  • recap bottle after each use
  • keep away from heat or direct sunlight
  • store at room temperature 15° – 25°C (59° – 77°F)
  • do not use if foil seal imprinted with "SEALED FOR YOUR PROTECTION" under cap is broken or missing
  • keep carton for full drug facts

Inactive ingredient

INACTIVE INGREDIENT SECTION

glycerin

Questions? 

OTC - QUESTIONS SECTION

1-800-344-7239 Aurodri.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

29.6 mL Bottle Carton
AURO- DRI®
ISOPROPYL ALCOHOL 95% in an
ANHYDROUS GLYCERIN 5% base

– Ear Drying Aid

CLEARS WATER FROM 
SWIMMERS' EARS

1 FL OZ (29.6 mL)

PRINCIPAL DISPLAY PANEL 29.6 mL Bottle Carton AURO- DRI® ISOPROPYL ALCOHOL 95% in an ANHYDROUS GLYCERIN 5% base – Ear Drying Aid CLEARS WATER FROM SWIMMERS' EARS Helps relieve c...PRINCIPAL DISPLAY PANEL 29.6 mL Bottle Carton AURO- DRI® ISOPROPYL ALCOHOL 95% in an ANHYDROUS GLYCERIN 5% base – Ear Drying Aid CLEARS WATER FROM SWIMMERS' EARS Helps relieve c...

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Isopropyl AlcoholACTIVE INGREDIENTND2M4163021
Isopropyl AlcoholACTIVE MOIETYND2M4163021
GlycerinINACTIVE INGREDIENTPDC6A3C0OX1

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
63736-32763736-327-24, 63736-327-12

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
ISOPROPYL ALCOHOLND2M416302ACTIB
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-10-25full-release2026-06-01 00:33:57

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 15 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GlycerinGLYCERINPDC6A3C0OXSOLUTION / AURICULAR (OTIC)63.64 %w/vExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION / AURICULAR (OTIC)63.64 %w/vExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION/ DROPS / AURICULAR (OTIC)25 mgExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXLIQUID / TOPICAL2.5 %w/wExact identifier — unii+dosage form
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXLIQUID / TOPICAL2.5 %w/wExact identifier — unii+dosage form
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSUSPENSION / AURICULAR (OTIC)0.05 %w/wExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION/ DROPS / AURICULAR (OTIC)25 mgExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSUSPENSION / AURICULAR (OTIC)0.05 %w/wExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+dosage form
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXLIQUID / TOPICAL2.5 %w/wExact identifier — unii+dosage form
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+dosage form
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION/ DROPS / AURICULAR (OTIC)25 mgExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSUSPENSION / AURICULAR (OTIC)0.05 %w/wExact identifier — unii+route
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+dosage form
15 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION / AURICULAR (OTIC)63.64 %w/vExact identifier — unii+route
15 equally ranked IID candidates

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
69011005-7548-4563-93a1-bf7e561f6c9885cb4973-6a81-4d8f-b187-4bf709d93a982024-10-25WarningsExact identifier
spl set id: 85cb4973-6a81-4d8f-b187-4bf709d93a98

Reported adverse events (FAERS/openFDA)#

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