Walgreens Muro 128 Drops 0.5 oz 877987 (2018)

Manufacturer
Walgreens, Co.
Effective date
2018-03-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:00:49

Label at a glance#

ProductWalgreens Muro 128
Active ingredientSODIUM CHLORIDE
Label structure11 sections

Storage and handling

Other information store upright at 15°-25°C (59°-77°F) keep tightly closed

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Sodium chloride 5%................................................Hypertonicity agent

OTC - PURPOSE SECTION

Uses

  • temporary relief of corneal edema

WARNINGS SECTION

Warnings

Do not use

  • except under the advice and supervision of a doctor
  • if solution changes color or becomes cloudy

OTC - WHEN USING SECTION

When using this product

  • it may cause temporary burning and irritation
  • to avoid contamination do not touch tip of container to any surface
  • replace cap after use

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens or persists for more than 72 hours
  • you experience eye pain, changes in vision, continued redness or irritation of the eye

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Directions

  • instill 1 to 2 drops in the affected eye(s) every 3 or 4 hours, or as directed by a physican

STORAGE AND HANDLING SECTION

Other information

  • store upright at 15°-25°C (59°-77°F)
  • keep tightly closed

INACTIVE INGREDIENT SECTION

Inactive ingredients

boric acid, hydrochloric acid, hypromellose, methylparaben, propylene glycol, propylparaben, sodium borate, sodium hydroxide, purified water

DOSAGE & ADMINISTRATION SECTION

Distributed by:

200 Wilmot Rd.

Deerfield, IL 60015

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-38000363-3800-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
c9de073b-9c34-0e5c-e053-2995a90a75ff67e057a5-c6a8-3e42-e053-2a91aa0a51e32021-08-18WarningsExact identifier
spl set id: 67e057a5-c6a8-3e42-e053-2a91aa0a51e3

Reported adverse events (FAERS/openFDA)#

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