MURINE TEARS FOR DRY EYES- polyvinyl alcohol and povidone liquid 
Prestige Brands Holdings, Inc.

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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Murine Tears for Dry Eyes

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)



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)

MURINE TEARS FOR DRY EYES 
polyvinyl alcohol and povidone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-574
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED5 mg  in 1 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C16) (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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-574-011 in 1 BOX10/01/201210/28/2022
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/01/201210/28/2022
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 3/2023
 
Prestige Brands Holdings, Inc.