FDA.reportPublic FDA data

Murine Plus for Dry Eyes Redness Relief

Manufacturer
Prestige Brands Holdings, Inc.
Effective date
2024-10-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:50:39

Label at a glance#

ProductMurine Plus for Dry Eyes Redness Relief
Active ingredientPOLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

for the temporary relief of burning & irritation due to dryness of the eye for use as a protectant against further irritation or to relieve dryness of the eye relieves redness of the eye due to minor eye irritations

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Polyvinyl alcohol 0.5%

Povidone 0.6%

Tetrahydrozoline hydrochloride 0.05%            

Purpose

OTC - PURPOSE SECTION

Lubricant

Lubricant

Redness reliever

Uses

INDICATIONS & USAGE SECTION

  • for the temporary relief of burning & irritation due to dryness of the eye
  • for use as a protectant against further irritation or to relieve dryness of the eye
  • relieves redness of the eye due to minor eye irritations

Warnings

WARNINGS SECTION

For external use only

Do not use if

OTC - DO NOT USE SECTION

solution changes color or becomes cloudy.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

narrow angle glaucoma.

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

OTHER SAFETY INFORMATION

  • store at 20°-25°C (68°-77°F)
  • remove contact lenses before using

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67172-573MURINE PLUS FOR DRY EYES REDNESS RELIEF (POLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [PRESTIGE BRANDS HOLDINGS, INC.]4Legacy NDC20241102_2c2ffa09-bcbb-483b-830a-ac63e9893de4.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67172-573-15ML - Milliliter67172-573ff3ccca7-5eeb-48b0-bd1b-18fe4819c33112022-06-06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67172-57367172-573-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYVINYL ALCOHOL, UNSPECIFIED532B59J990ACTIB
POVIDONEFZ989GH94EACTIB
TETRAHYDROZOLINE HYDROCHLORIDE0YZT43HS7DACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
DEXTROSEIY9XDZ35W2IACT
EDETATE DISODIUM7FLD91C86KIACT
POTASSIUM CHLORIDE660YQ98I10IACT
SODIUM BICARBONATE8MDF5V39QOIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM CITRATE1Q73Q2JULRIACT
SODIUM PHOSPHATE, DIBASICGR686LBA74IACT
SODIUM PHOSPHATE, MONOBASIC3980JIH2SWIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4d6a925b-8b63-45fd-a302-a44514e341f52c2ffa09-bcbb-483b-830a-ac63e9893de42026-01-09WarningsExact identifier
spl set id: 2c2ffa09-bcbb-483b-830a-ac63e9893de4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.