AURO DRI- isopropyl alcohol liquid 
Insight Pharmaceuticals LLC

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.

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Auro Dri

AURO-DRI ®

Drug Facts

Active ingredient

Isopropyl alcohol 95% in an anhydrous glycerin 5% base

Purpose

Ear drying aid

Use

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

Warnings

Flammable

Keep away from fire or flame

Do not use

in the eyes

Ask a doctor before use if you have

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

Stop use and ask a doctor if

irritation (too much burning) or pain occurs

Keep out of reach of children.

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

Directions

Other information 

Inactive ingredient

glycerin

Questions? 

1-800-344-7239 Aurodri.com

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 clogged ear
discomfort due to bathing,
showering and swimming
Safe for children
1 FL OZ (29.6 mL)

AURO DRI 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-327
Route of AdministrationAURICULAR (OTIC)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL95 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
Product Characteristics
ColorWHITE (Clear) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63736-327-2424 in 1 CASE06/14/2010
11 in 1 BOX
129 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:63736-327-1212 in 1 CASE06/14/2010
21 in 1 BOX
229 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34406/14/2010
Labeler - Insight Pharmaceuticals LLC (055665422)

Revised: 1/2020
Document Id: c540e5e0-8ba7-4c0f-b333-290fde2cef65
Set id: 85cb4973-6a81-4d8f-b187-4bf709d93a98
Version: 4
Effective Time: 20200110
 
Insight Pharmaceuticals LLC