RETAINE NACL- sodium chloride, lanolin alcohols, mineral oil, water, petrolatum ointment

Retaine NaCl by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

• Active ingredient: Purpose
• Sodium chloride (5%): Hypertonicity agent

Use

For the temporary relief of corneal edema.

Warnings

For use in the eyes only.

Do not use

• except under the advice and supervision of a doctor. 

When using this product

• it may cause temporary burning and irritation.
• do not touch tip of container to any surface to avoid contamination.
• replace cap after use.

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 72 hours.

Keep out of reach of children.

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

Directions

• Pull down the lower lid of the affected eye(s).
• Apply a small amount (¼ inch) of ointment to the inside of the eyelid every 3-4 hours or as directed by a doctor.

Other information

• Do not use if imprinted carton seals are not intact.
• Store at 15°- 30°C (59°- 86°F).
• Keep cap tightly closed.
• Retain carton for complete drug facts.

Inactive ingredients

Lanolin alcohol, mineral oil, water for injection, white petrolatum.

Questions?

☎ Call (800) 233-5469
M-F 8:30AM-5:00PM CST or visit
www.retainebrand.com 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW!

NaCl™
OINTMENT

Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%

retaine®

OCuSOFT®

Sterile
Net wt. 1/8 oz
(3.5 g)

FOR USE IN THE EYES ONLY

OCuSOFT®

Distributed by
OCuSOFT, Inc.
Rosenberg, TX 77471 USA

© 2017 OCuSOFT, Inc.
® and ™ marks owned by OCuSOFT, Inc.
www.ocusoft.com

Made in the USA

Ini1014
R1117

#777-3-76

INGREDIENTS AND APPEARANCE

RETAINE NACL 
sodium chloride, lanolin alcohols, mineral oil, water, petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54799-894
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Chloride (UNII: 451W47IQ8X) (Chloride Ion - UNII:Q32ZN48698)	Sodium Chloride	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Lanolin Alcohols (UNII: 884C3FA9HE)
Mineral Oil (UNII: T5L8T28FGP)
Petrolatum (UNII: 4T6H12BN9U)
Water (UNII: 059QF0KO0R)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54799-894-35	1 in 1 CARTON	08/18/2015
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 final	part349	08/18/2015

Labeler - OCuSOFT, Inc. (174939207)

Registrant - OCuSOFT, Inc. (174939207)