CARBOXYMETHYLCELLULOSE SODIUM- carboxymethylcellulose sodium solution/ drops 
AvPAK

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Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%
(preservative free)

Lubricant Eye Drops

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses    

Warnings

Stop use and ask a doctor if

you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

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

Other information

Inactive ingredients

Calcium chloride; hydrochloric acid; magnesium chloride; potassium chloride; purified water; sodium chloride; sodium hydroxide and sodium lactate.

Questions or comments?

1-855-361-3993

PRINCIPAL DISPLAY PANEL

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CARBOXYMETHYLCELLULOSE SODIUM 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50268-067
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
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50268-067-3030 in 1 CARTON11/19/2020
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:50268-067-5050 in 1 CARTON11/19/2020
20.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
3NDC:50268-067-7070 in 1 CARTON11/19/2020
30.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01811/19/2020
Labeler - AvPAK (832926666)

Revised: 3/2024
Document Id: 130358f4-1b61-5b60-e063-6394a90aa1d5
Set id: b478a695-ded0-2e5f-e053-2995a90ac45e
Version: 5
Effective Time: 20240306
 
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