Auro-Dri

Dosage form: liquid
Ingredients: Isopropyl Alcohol 28mL in 29mL
Labeler: Insight Pharmaceuticals
NDC Code: 63736-327

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.

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

  • swimming
  • showering
  • bathing
  • washing the hair

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
  • 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
  • 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

Questions?

call 1-800-344-7239

Vist our website at www.aurodri.com

Distributed by: INSIGHT Pharmaceuticals Corp.
Langhorne, PA 19047-1749

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)DEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Isopropyl Alcohol (Isopropyl Alcohol) Isopropyl Alcohol28 mL  in 29 mL
Inactive Ingredients
Ingredient NameStrength
Glycerin1 mL  in 29 mL
Product Characteristics
ColorWHITE (Clear) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63736-327-2424 BOX (BOX) in 1 CASE
11 BOTTLE (BOTTLE) in 1 BOX
129 mL in 1 BOTTLE
2NDC:63736-327-1212 BOX (BOX) in 1 CASE
21 BOTTLE (BOTTLE) in 1 BOX
229 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34406/14/2010
Labeler - Insight Pharmaceuticals (176792315)

Revised: 06/2010
 
Insight Pharmaceuticals

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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