RETAINE NACL- boric acid, hypromelloses, methylparaben, propylene glycol, propylparaben, sodium borate, water, sodium hydroxide and/or hydrochloric acid solution

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. 
• if solution changes color or becomes cloudy.

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.
• remove contact lenses before using.

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 more than 72 hours.

Keep out of reach of children.

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

Directions

• Instill 1 or 2 drops in the affected eye(s).
• Apply every 3 or 4 hours or as directed by a doctor.

Other information

• Retain carton for complete drug facts
• Do not use if imprinted seal on cap is torn.
• Store at room temperature 15°-20°C (59°-86°F).
• Keep cap tightly closed.

Inactive ingredients

Boric acid, hypromellose, methylparaben, propylene glycol, propylparaben, sodium borate and water for injection. Sodium hydroxide and/or hydrochloric acid may be added to adjust pH.

Questions?

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW!

NaCl™
OPHTHALMIC SOLUTION

Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%

retaine®

OCuSOFT®

Sterile
0.5 FL OZ (15 mL)

FOR USE IN THE EYES ONLY

OCuSOFT®

Manufactured for OCuSOFT, Inc.
Rosenberg, TX 77471 USA

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

Made in the USA

Ini1014
#777-3-77
R1117

INGREDIENTS AND APPEARANCE

RETAINE NACL 
boric acid, hypromelloses, methylparaben, propylene glycol, propylparaben, sodium borate, water, sodium hydroxide and/or hydrochloric acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54799-895
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 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)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54799-895-35	1 in 1 CARTON	08/28/2015
1		15 mL in 1 BOTTLE, DROPPER; 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	08/28/2015

Labeler - OCuSOFT, Inc. (174939207)

Registrant - OCuSOFT, Inc. (174939207)