CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5%- carboxymethylcellulose sodium eye drops 0.5% for solution 
Aurolab

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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Active ingredient

Carboxymethyl cellulose sodium Eye Drops 0.5% w/v

DIRECTIONS FOR USE

INACTIVE INGREDIENT

1.Boric acid

2.Calcium chloride

3.Glycerin
4.Magnesium chloride

5.Mannitol

6.Potassium chloride

7.Purified water

8.Stablized oxy cholro complex

9.Sodium tetra borate
10.Sodium hyaluronate

11.Sodium citrate

Tamper Protection

Use

For use as a lubricant to prevent further irritation or to relieve dryness of the eye

Questions

Call. 1-800-103-7321
E-mail : info@aurolab.com
Web : www.aurolab.com

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away

Stop use and ask a doctor if

1.Excessive watering of the eye

2.Burning, stinging,foreign body sensation Continued redness (or) irritation of the eye, unusual eye secretions, change in vision

Do not use

1.If you are sensitive to any ingredient in this product
2.If solution changes color or becomes cloudy

Warnings

For external use only

Indication & usage

Do not touch the nozzle tip to any surface since this may contaminate the solution
Remove contact lenses before use Should not use at the same time as other ophthalmic drugs
Replace cap after using

Dose

Instill 1 or 2 drops in the affected eyes as needed

Eye lubricant

Eye lubricant

Carton

CMC NAHY

CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5% 
carboxymethylcellulose sodium eye drops 0.5% for solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16030-501
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM CHLORITE (UNII: G538EBV4VF)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
MANNITOL (UNII: 3OWL53L36A)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16030-501-055 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/20/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/20/2022
Labeler - Aurolab (677319965)
Establishment
NameAddressID/FEIBusiness Operations
Aurolab677319965manufacture(16030-501)

Revised: 8/2023
Document Id: 039b9ee7-e910-f323-e063-6294a90ab428
Set id: e8b4df3b-3d81-b3ca-e053-2a95a90af2ec
Version: 4
Effective Time: 20230823
 
Aurolab