OTC Medication Information: Auro Dri

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.

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

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’ EARS1 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)
(click image for full-size original)
AURO DRI isopropyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-327
Route of Administration AURICULAR (OTIC) DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 95 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
Product Characteristics
Color WHITE (Clear) Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63736-327-24 24 BOX in 1 CASE contains a BOX
1 1 BOTTLE in 1 BOX This package is contained within the CASE (63736-327-24) and contains a BOTTLE
1 29 mL in 1 BOTTLE This package is contained within a BOX and a CASE (63736-327-24)
2 NDC:63736-327-12 12 BOX in 1 CASE contains a BOX
2 1 BOTTLE in 1 BOX This package is contained within the CASE (63736-327-12) and contains a BOTTLE
2 29 mL in 1 BOTTLE This package is contained within a BOX and a CASE (63736-327-12)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part344 06/14/2010
Labeler — Insight Pharmaceuticals LLC (055665422)

Revised: 01/2020 Insight Pharmaceuticals LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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