SODIUM CHLORIDE HYPERTONICITY- sodium chloride ointment

SODIUM CHLORIDE HYPERTONICITY by

Drug Labeling and Warnings

SODIUM CHLORIDE HYPERTONICITY by is a Otc medication manufactured, distributed, or labeled by YYBA CORP, Bausch & Lomb Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium chloride 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 provided below 

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

Questions or comments?

Call 1-866-933-6337

Package/Label Principal Display Panel

Welmate TM

NDC: 73581-708-35

EYE OINTMENT

sodium chloride hypertonicity

ophthalmic ointment, 5%

5%Temporary Relief
of Corneal Edema

STERILE

NET WT. 1/8 OZ. (3.5 g)

9805700

WM15834

INGREDIENTS AND APPEARANCE

SODIUM CHLORIDE HYPERTONICITY 
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73581-708
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
LANOLIN (UNII: 7EV65EAW6H)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73581-708-35	1 in 1 CARTON	08/12/2024
1		3.5 mL 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	08/12/2024

Labeler - YYBA CORP (006339772)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		079587625	manufacture(73581-708)