SOCHLOR- sodium chloride hypertonicity ophthalmic ointment 5% sterile ointment

Sochlor by

Drug Labeling and Warnings

Sochlor by is a Otc medication manufactured, distributed, or labeled by OCuSOFT, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

Sodium Chloride 5% (50mg)

PURPOSE:

Eye Lubricant

USES:

● for the temporary releif of corneal edema.

WARNINGS

For use in the eyes only.
● save box for complete warning information.

DO NOT USE:

● this product except under the advice and supervision of a doctor.

WHEN USING THIS PRODUCT:

● avoid contamination, do not touch tip of continer to any surface.
● replace cap after each use.
● this product may cause temporary burning and irritation on being instilled in the eye.

STOP USE AND ASK A DOCTOR IF:

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

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN:

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

DIRECTIONS:

● Apply a small amount (one-fourth inch) of ointment to the inside of the affected eye(s) every 3-4 hours, or as directed
by a doctor.

OTHER INFORMATION:

● Store at room temperature 15°-30°C (59°-86°F).
● keep from freezing.
● keep tightly closed.
● See crimp of tube or box for lot number and expiration date.

INACTIVE INGREDIENT:

Lanolin Oil, Mineral Oil, Water for Injection and White Petrolatum.

QESTIONS OR COMMENTS?

281-342-3350 or consult www.ocusoft.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOCHLOR  
sodium chloride hypertonicity ophthalmic ointment 5% sterile ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54799-926
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 Oil (UNII: OVV5IIJ58F)
Mineral Oil (UNII: T5L8T28FGP)
Water (UNII: 059QF0KO0R)
Petrolatum (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54799-926-35	3.5 g in 1 TUBE; Type 0: Not a Combination Product	02/05/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	02/05/2014

Labeler - OCuSOFT, Inc. (174939207)