Murine Plus 2

Manufacturer
Prestige Brands Holdings, Inc.
Effective date
2021-01-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:56:13

Label at a glance#

ProductMurine Plus 2
Active ingredientTETRAHYDROZOLINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

removes redness of the eyes relieves minor eye irritation due to swimming, wind, dust, and close work gently soothing and refreshing irritated eyes

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 ingredient

OTC - ACTIVE INGREDIENT SECTION

Tetrahydrozoline hydrochloride 0.05%

Purpose

OTC - PURPOSE SECTION

Redness reliever

Uses

INDICATIONS & USAGE SECTION

  • removes redness of the eyes
  • relieves minor eye irritation due to swimming, wind, dust, and close work
  • gently soothing and refreshing irritated eyes

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if 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

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 room temperature
  • remove contact lenses before using

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride 0.01% (preservative), edetate disodium 0.1% (preservative). 

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Murine Plus 2

Redness Relief

15ml

PRINCIPAL DISPLAY PANEL Murine Plus 2 Redness Relief 15mlPRINCIPAL DISPLAY PANEL Murine Plus 2 Redness Relief 15ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67172-402-152023-11-09C16284748780-1f386c649-c672-0266-e053-dadaa90a7c1aMurine Plus 2 - Redness Relief
67172-402-152023-01-30C16284748780-1f386c649-c672-0266-e053-dadaa90a7c1aMurine Plus 2 - Redness Relief

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67172-40267172-402-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
7188badc-99d4-436d-90d1-53c657ad1c1b44f135ab-365c-48ca-948b-763cb9fd2b792023-11-13WarningsExact identifier
spl set id: 44f135ab-365c-48ca-948b-763cb9fd2b79

Reported adverse events (FAERS/openFDA)#

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