SOCHLOR- sodium chloride hypertonicity ophthalmic solution 5% solution solution/ drops

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%

Purpose

Hypertonicity eye drop

Do not use

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

Use

● for the temporary releif of corneal edema

Warnings

For use in the eye(s) only.

When using this product

● avoid contamination, do not touch tip of container to any surface.
● replace cap after each use.
● may cause temporary burning and irritation on being instilled into 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 OUT OF THE REACH OF CHILDREN.

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

Directions

● instill 1 or 2 drops in the affected eye(s) every 3-4 hours, or as directed by a doctor.

Other information

● keep carton for complete product information
● Store at room temperature 15°-30°C (59°-86°F).
● keep tightly closed

Inactive ingredients

● Boric Acid, Hypromellose, Methylparaben, Propylene Glycol, Propylparaben, Sodium Borate,
and Water for injection. Sodium Hydroxide and/or Hydrochloride Acid may be added to adjust pH.

Questions or comments?

Call (800) 233-5469 M-F 8:30AM - 5:30PM CST

DO NOT USE IF IMPRINTED SEAL ON CAP IT TORN, BROKEN OR MISSING AND
IMPRINTED CARTON SEALS ARE NOT INTACT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOCHLOR  
sodium chloride hypertonicity ophthalmic solution 5% solution solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54799-925
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
Boric Acid (UNII: R57ZHV85D4)
Hypromelloses (UNII: 3NXW29V3WO)
Methylparaben (UNII: A2I8C7HI9T)
Propylene Glycol (UNII: 6DC9Q167V3)
Propylparaben (UNII: Z8IX2SC1OH)
Sodium Borate (UNII: 91MBZ8H3QO)
Water (UNII: 059QF0KO0R)
Sodium Hydroxide (UNII: 55X04QC32I)
Hydrochloric Acid (UNII: QTT17582CB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54799-925-15	15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	02/03/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	02/03/2014

Labeler - OCuSOFT, Inc. (174939207)