CARBOXYMETHYLCELLULOSE SODIUM- carboxymethylcellulose sodium solution/ drops 
AvPAK

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Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%

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.

Directions

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Inactive ingredients

Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate; and sodium chloride. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or comments?

1-855-361-3993

PRINCIPAL DISPLAY PANEL

68

CARBOXYMETHYLCELLULOSE SODIUM 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50268-068
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORITE (UNII: G538EBV4VF)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
SODIUM CHLORATE (UNII: T95DR77GMR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50268-068-151 in 1 CARTON11/19/2020
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 DrugM01811/19/2020
Labeler - AvPAK (832926666)

Revised: 3/2024
Document Id: 13036b90-42c9-5cee-e063-6394a90a8c15
Set id: b479d2ae-4b59-916a-e053-2995a90af8ec
Version: 6
Effective Time: 20240306
 
AvPAK