MURINE PLUS FOR DRY EYES REDNESS RELIEF- polyvinyl alcohol and povidone and tetrahydrozoline hydrochloride solution/ drops 
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 Plus for Dry Eyes Redness Relief

Drug Facts

Active ingredients

Polyvinyl alcohol 0.5%

Povidone 0.6%

Tetrahydrozoline hydrochloride 0.05%            

Purpose

Lubricant

Lubricant

Redness reliever

Uses

Warnings

For external use only

Do not use if

solution changes color or becomes cloudy.

Ask a doctor before use if you have

narrow angle glaucoma.

When using this product

  • to avoid contamination, do not touch tip to any surface
  • replace cap after using
  • overuse may produce increased redness of the eye
  • pupils may become enlarged temporarily

Stop use & 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 last for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Other information

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® PLUS for DRY EYES Redness Reliever
Lubricant/Redness Reliever Eye Drops
0.5 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL
Murine® PLUS for DRY EYES Redness Reliever
Lubricant/Redness Reliever Eye Drops
0.5 FL OZ (15 mL)

MURINE PLUS FOR DRY EYES REDNESS RELIEF 
polyvinyl alcohol and povidone and tetrahydrozoline hydrochloride solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-573
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
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
DEXTROSE (UNII: IY9XDZ35W2)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-573-1515 mL in 1 BOTTLE; Type 0: Not a Combination Product03/07/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34903/07/2017
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 12/2021
Document Id: 5c34fc5b-f953-4c4f-898c-72c5f8120e44
Set id: 2c2ffa09-bcbb-483b-830a-ac63e9893de4
Version: 3
Effective Time: 20211222
 
Prestige Brands Holdings, Inc.