AURO DRI- isopropyl alcohol liquid

Auro Dri by

Drug Labeling and Warnings

Auro Dri by is a Otc medication manufactured, distributed, or labeled by Insight Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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' EARS
1 FL OZ (29.6 mL)

INGREDIENTS AND APPEARANCE

AURO DRI 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63736-327
Route of Administration	AURICULAR (OTIC)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	95 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)

Product Characteristics
Color	WHITE (Clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63736-327-24	24 in 1 CASE	06/14/2010
1		1 in 1 BOX
1		29 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 63736-327-12	12 in 1 CASE	06/14/2010
2		1 in 1 BOX
2		29 mL in 1 BOTTLE; Type 0: Not a Combination Product

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)