Skip to Content

← See all Sochlor brands

Sochlor by OCuSOFT, Inc.

Dosage form: ointment
Ingredients: Sodium Chloride 50mg in 1g
Labeler: OCuSOFT, Inc.
NDC Code: 54799-926

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Sochlor™

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

SOCHLOR  
sodium chloride hypertonicity ophthalmic ointment 5% sterile ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54799-926
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Chloride (Sodium Cation) Sodium Chloride50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Lanolin Oil 
Mineral Oil 
Water 
Petrolatum 
Packaging
#Item CodePackage Description
1NDC:54799-926-353.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/05/2014
Labeler - OCuSOFT, Inc. (174939207)

 
OCuSOFT, Inc.

← See all Sochlor brands

Medically reviewed on Feb 5, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide