LUBRICATING EYE DROPS- carboxymethylcellulose sodium liquid 
A2A Integrated Pharmaceuticals, LLC

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                                                                    Purpose

Carboxymethylcellulose sodium 0.5%------------------------- Eye lubricant

Uses

Warnings

For external use only

• Do not use if solution changes color or becomes cloudy.

When using this product

to avoid contamination, do no touch tip of container to any surface. Do not reuse. Once open, discard.

Do not touch unit dose tip to eye.

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

■ TWIST AND REMOVE TAB.

■ Place 1 or 2 drops in the affected eye(s) as needed for relief and discard container.
■ If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions.

Inactive Ingredients

Calcium chloride, hydrochloric acid*, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide*, and sodium
lactate.*May or may not contain this ingredient to adjust pH.

Other information

■ Use only if single-use container is intact.
■ Use before expiration date marked on container.
■ RETAIN THIS FOIL FOR FUTURE REFERENCE.

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LUBRICATING EYE DROPS 
carboxymethylcellulose sodium liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73141-001
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
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73141-001-018 in 1 CARTON10/04/2019
10.6 mL in 1 AMPULE; Type 0: Not a Combination Product
2NDC:73141-001-0232 in 1 CARTON10/04/2019
20.6 mL in 1 AMPULE; Type 0: Not a Combination Product
3NDC:73141-001-0352 in 1 CARTON10/04/2019
30.6 mL in 1 AMPULE; Type 0: Not a Combination Product
4NDC:73141-001-0472 in 1 CARTON10/04/2019
40.6 mL in 1 AMPULE; Type 0: Not a Combination Product
5NDC:73141-001-05100 in 1 CARTON10/04/2019
50.6 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/04/2019
Labeler - A2A Integrated Pharmaceuticals, LLC (117064671)

Revised: 10/2019
Document Id: addbf328-1531-40cc-b40c-b10df5911f9a
Set id: 77387733-3350-4dad-9812-38854e9cf760
Version: 2
Effective Time: 20191007
 
A2A Integrated Pharmaceuticals, LLC