RETAINE CMC LUBRICANT EYE DROPS - carboxymethylcellulose sodium solution
OCuSOFT Inc.

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.

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Drug Facts

Active Ingredient

Carboxymethylcellulose sodium 0.5%................................. Eye Lubricant

Uses

Relieves dryness of the eye.
Temporarily relieves discomfort due to minor irritations of the eye or from exposure to wind or sun.
As a protectant against further irritation.

Warnings

For use in the eyes only.
Do not use if solution changes color or becomes cloudy.

When using this product

do not touch tip of container to any surface to avoid contamination.
do not reuse once opened.

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 immediately.

Directions

To open, TWIST AND PULL TAB TO REMOVE.
Instill 1 or 2 drops into affected eye(s) as needed and discard container.

Other Information

Use only if printed tamper seals on top and bottom flaps are intact.
Use only if twist top of single-dose container is intact.
Store between 15º-30ºC (59º-86ºF).

Inactive Ingredients

Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions

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

Purpose

Eye Lubricant

RETAINE CMC LUBRICANT EYE DROPS
carboxymethylcellulose sodium solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54799-897
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LACTATE (UNII: TU7HW0W0QT)
WATER (UNII: 059QF0KO0R)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54799-897-30	30 in 1 CONTAINER	09/01/2011	04/30/2019
1		0.4 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	09/01/2011	04/30/2019

Labeler - OCuSOFT Inc. (174939207)

Name	Address	ID/FEI	Business Operations
Establishment
Altaire Pharmaceuticals, Inc.		786790378	manufacture(54799-897)

Revised: 10/2021

Document Id: 0794f6a0-f6c7-4da3-bf27-65546f2bc89c

Set id: 6b40c38e-31f8-4aca-9456-04128e6c2e93

Version: 5

Effective Time: 20211025

OCuSOFT Inc.