CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC SOLUTION 0.5%- carboxymethylcellulose sodium solution/ drops 
EMC Pharma, LLC

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Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Use

• For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun.
• May be used as 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

• Avoid contamination, do not touch tip of container to any surface.
• 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 more than 72 hours

Keep this and all drugs out of the reach of the children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222)

Directions

• Shake well before use.
• Instill 1 or 2 drops in the affected eye(s) as needed.

Other Information

• Store at room temperature 15°- 30 ° (59 °- 86 °F).
• Do Not Use if imprinted seal on cap is torn, broken or missing.
• Discard 90 days after opening
• Retain outer carton for full product drug information

Inactive Ingredient

Boric Acid, Calcium Chloride, Magnesium Chloride, Potassium Chloride, Purified water, Sodium borate, Sodium Chloride. Stabilized Oxychloro Complex 2.5%. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or Comments?

• 1-855-317-1107

Distributed By:
EMC Pharma, LLC
11551 Adie Rd, Maryland Heights, MO 63043

Rev. 10/2021

Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% (NDC 81288-798-15)

image description

CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC SOLUTION 0.5% 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81288-798
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
Magnesium Chloride (UNII: 02F3473H9O)  
Potassium Chloride (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
Sodium borate (UNII: 91MBZ8H3QO)  
Sodium Chloride (UNII: 451W47IQ8X)  
Hydrochloric Acid (UNII: QTT17582CB)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81288-798-151 in 1 CARTON01/01/202203/05/2024
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01801/01/202203/05/2024
Labeler - EMC Pharma, LLC (117754047)
Registrant - EMC Pharma, LLC (117754047)

Revised: 3/2024
 
EMC Pharma, LLC