MURINE TEARS PLUS 3- polyvinyl alcohol, povidone and tetrahydrozoline hydrochloride liquid

Murine Tears Plus 3 by

Drug Labeling and Warnings

Murine Tears Plus 3 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 ingredients

Polyvinyl alcohol 0.5%

Active ingredients

Povidone 0.6%

Purpose

Lubricant

Active ingredient

Tetrahydrozoline hydrochloride 0.05%

Purpose

Redness reliever

Uses

• temporarily relieves irritation due to dryness of the eye
  
• provides soothing relief from minor eye irritations
  
• removes redness from the eye

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

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

Stop use & ask a doctor if

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

Keep out of reach of children.

Directions

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

Other information

• store at room temperature
  
• remove contact lenses before using

Inactive ingredients

benzalkonium chloride 0.005% (preservative), dextrose, disodium edetate, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, and sodium phosphate (mono- and dibasic).

PRINCIPAL DISPLAY PANEL

Murine Tears Plus 3
15 mL

INGREDIENTS AND APPEARANCE

MURINE TEARS PLUS 3 
polyvinyl alcohol, povidone and tetrahydrozoline hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67172-403
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
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077)	TETRAHYDROZOLINE HYDROCHLORIDE	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
DEXTROSE (UNII: IY9XDZ35W2)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67172-403-15	1 in 1 BOX	03/15/2011
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
EXPORT ONLY		03/15/2011

Labeler - Prestige Brands Holdings, Inc. (159655021)