WALGREENS MURO 128- sodium chloride solution/ drops

Walgreens Muro 128 by

Drug Labeling and Warnings

Walgreens Muro 128 by is a Otc medication manufactured, distributed, or labeled by Walgreens, Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

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

PURPOSE

Uses

• temporary relief of corneal edema

WARNINGS

Warnings

Do not use

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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

Other information

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

INACTIVE INGREDIENT

Inactive ingredients

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

DOSAGE & ADMINISTRATION

Distributed by:

200 Wilmot Rd.

Deerfield, IL 60015

Made in South Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS MURO 128 
sodium chloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-3800
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM BORATE (UNII: 91MBZ8H3QO)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
BORIC ACID (UNII: R57ZHV85D4)
HYDROCHLORIC ACID (UNII: QTT17582CB)
METHYLPARABEN (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-3800-15	1 in 1 BOX	03/20/2018
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
OTC monograph final	part349	03/20/2018

Labeler - Walgreens, Co. (008965063)