MURINE TEARS FOR DRY EYES- polyvinyl alcohol and povidone liquid

Murine Tears for Dry Eyes by

Drug Labeling and Warnings

Murine Tears for Dry Eyes by is a Otc medication manufactured, distributed, or labeled by Prestige Brands Holdings, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Polyvinyl alcohol 0.5%

Purpose

Lubricant

Active ingredient

Povidone 0.6%

Purpose

Lubricant

Uses

• For the temporary relief of burning & irritation due to dryness of the eye.
  
• For use as a protectant against further irritation or dryness of the eye.

Warnings

For external use only.

Do not use

if solution changes color or becomes cloudy.

When using this product

• to avoid contamination, do not touch tip of container to any surface.
  
• recap cap after using.

Stop use and ask a doctor if:

• you experience eye pain
  
• you experience changes in vision
  
• you experience continued redness or irritation of the eye
  
• the condition worsens
  
• symptoms lasts for more than 72 hours        

Keep out of reach of children.

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

Directions

Instill 1 to 2 drops in the affected eye(s) as needed.

Other information

• store at 20°- 25°C (68°-77°F)
  
• remove contact lenses before using
  
• Tamper Evident: Do not use if neckband on bottle is broken or missing.

Inactive ingredients

benzalkonium chloride, dextrose, edetate disodium, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate (mono- and dibasic)

Questions?

1-877-854-0853 www.murine.com

PRINCIPAL DISPLAY PANEL

Murine
Tears® For DRY EYES
Lubricant Eye Drops
Original Natural Tears Formula
● Moisture Enriched
● Eye Doctor Recommended
0.5 fl oz. (15 mL)

INGREDIENTS AND APPEARANCE

MURINE TEARS FOR DRY EYES 
polyvinyl alcohol and povidone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67172-574
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990)	POLYVINYL ALCOHOL, UNSPECIFIED	5 mg  in 1 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E)	POVIDONE	6 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
DEXTROSE (UNII: IY9XDZ35W2)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM PHOSPHATE (UNII: SE337SVY37)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67172-574-01	1 in 1 BOX	10/01/2012
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part349	10/01/2012

Labeler - Prestige Brands Holdings, Inc. (159655021)