Carboxymethylcellulose Sodium Eye Drops 0.5%

Manufacturer
Aurolab
Effective date
2026-01-27
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:35:09

Label at a glance#

ProductCarboxymethylcellulose Sodium Eye Drops 0.5%
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Label structure14 sections

Dosage and administration

lnstill 1or 2 drops in the affected eye, as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Carboxymethyl cellulose sodium Eye Drops 0.5% w/v

DIRECTIONS FOR USE

INSTRUCTIONS FOR USE SECTION

  • lnstill 1or 2 drops in the affected eye, as needed

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

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

OTHER SAFETY INFORMATION

  • For your protection a tamper evident ring is attached to the bottlecap
  • Upon opening, this will separate from the cap and can be discarded
  • Use only if this ring is present and attached when the bottle is first opened

Use

INDICATIONS & USAGE SECTION

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

Questions

OTC - QUESTIONS SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

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

OTC - DO NOT USE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Indication & usage

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Instill 1 or 2 drops in the affected eyes as needed

Eye lubricant

OTC - PURPOSE SECTION

Eye lubricant

Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CMC NAHYCMC NAHY

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionPSN9
1188426carboxymethylcellulose sodium 5 MG/ML Ophthalmic SolutionSCD9
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionSY9
1188426carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic SolutionSY9

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130803878065580GTIN-13: 0803878065580
EAN-13: 0803878065580
GTIN-12: 803878065580
UPC-A: 803878065580
GTIN storage (14 digits): 00803878065580
CMC0.5 NaHY.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
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7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
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810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
16030-501-05Carboxymethylcellulose Sodium Eye Drops 0.5%5 mL in 1 BOTTLE, DROPPERFOR SOLUTION59

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
16030-50116030-501-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Carboxymethylcellulose Sodium Eye Drops 0.5%CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5%Aurolabe8b4df3b-3d81-b3ca-e053-2a95a90af2ec2026-01-27WarningsExact identifier
ndc (package): 16030-501-05
ndc (product): 16030-501
ndc11 (package): 16030050105
spl id: 495c072a-fa45-45a7-e063-6394a90ad7d6
spl set id: e8b4df3b-3d81-b3ca-e053-2a95a90af2ec

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.