SODIUM CHLORIDE HYPERTONICITY- sodium chloride ointment

Sodium Chloride by

Drug Labeling and Warnings

Sodium Chloride by is a Otc medication manufactured, distributed, or labeled by CVS PHARMACY, Bausch & Lomb Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium chloride, 50 mg (5%)

Purpose

Hypertonicity agent

Uses

temporary relief of corneal edema

Warnings

For external use only

Do not use
▪except under the advice and supervision of a doctor

When using this product
▪it may cause temporary burning and irritation
▪replace cap after use
▪to avoid contamination do not touch tip of container to any surface

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.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

▪pull down the lower lid of the affected eye
▪apply a small amount (1/4 inch) of ointment to the inside of eyelid
▪apply every 3 or 4 hours or as directed by a doctor

Other information

▪store at 15°-25°C (59°-77°F)
▪keep tightly closed
▪ DO NOT FREEZE
▪see crimp of tube or carton for Lot Number and Expiration Date
▪do not use if difficult to dispense or visible particles are seen in the product
▪serious side effects associated with use of the product may be reported to the phone number below

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

Questions

[phone icon] Call 1-866-767-9161

Package/Label Principal Display Panel - Carton

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Compare to the active
ingredient in Muro 128 ®*

NDC 69842-285-35

Sodium Chloride
Hypertonicity
ophthalmic ointment, 5%
Temporary relief of corneal edema

NET WT 0.125 OZ (3.5 g)

STERILE

INGREDIENTS AND APPEARANCE

SODIUM CHLORIDE HYPERTONICITY 
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-285
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 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-285-35	1 in 1 CARTON	05/01/2020
1		3.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	05/01/2020

Labeler - CVS PHARMACY (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		079587625	manufacture(69842-285)