FDA.reportPublic FDA data

Medics Choice Lubricant Eye Drops

Manufacturer
K.C. Pharmaceuticals, Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:30:28

Label at a glance#

ProductMedics Choice Lubricant Eye Drops
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

carboxymethylcellulose sodium 0.5%

OTC - PURPOSE SECTION

Purpose

Carboxymethylcellulose sodium......Lubricant

INDICATIONS & USAGE SECTION

Uses

  • for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun
  • may be used as a protectant against further irritation

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use this product if

  • solution changes color or becomes cloudy

OTC - WHEN USING SECTION

When using this product

  • do not reuse
  • once opened, discard
  • to avoid contamination, do not touch tip of container to any surface
  • do not touch unit-dose tip to eye

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if

  • you experience eye pain
  • changes in vision occur
  • redness or irritation of the eye continues
  • redness or irritation of the eye worsens or persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • to open, twist and pull tab to remove
  • instill 1 or 2 drops in the affected eye(s) as needed and discard container
  • if used for post-operative (e.g., LASIK) dryness and discomfort, follow yur eye doctor's instructions

OTHER SAFETY INFORMATION

Other information

  • store at 15º-25ºC (59º-77ºF)
  • use only if single-use container is intact
  • use before expiration date marked on container
  • RETAIN THIS CARTON FOR FUTURE REFERENCE

INACTIVE INGREDIENT SECTION

Inactive ingredients

calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.

**may contain these ingredients to adjust pH.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CARTONCARTON

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionPSN4
1188426carboxymethylcellulose sodium 5 MG/ML Ophthalmic SolutionSCD4
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionSY4
1188426carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic SolutionSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130095072240010GTIN-13: 0095072240010
EAN-13: 0095072240010
GTIN-12: 095072240010
UPC-A: 095072240010
GTIN storage (14 digits): 00095072240010		MedicsChoiceLubEyeDr.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
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
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5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55651-030-01Medics Choice Lubricant Eye Drops0.4 mL in 1 AMPULESOLUTION0.44
55651-030-01Medics Choice Lubricant Eye Drops5 in 1 CARTONSOLUTION54

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55651-03055651-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311ACTIB
HYDROCHLORIC ACIDQTT17582CBIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
POTASSIUM CHLORIDE660YQ98I10IACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM LACTATETU7HW0W0QTIACT

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
Medics Choice Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMK.C. Pharmaceuticals, Inc.9ddfc275-602f-413b-e053-2995a90a11cb2025-12-30WarningsExact identifier
ndc (package): 55651-030-01
ndc (product): 55651-030
ndc11 (package): 55651003001
spl id: 4748c472-4128-0885-e063-6294a90a3b62
spl set id: 9ddfc275-602f-413b-e053-2995a90a11cb

Reported adverse events (FAERS/openFDA)#

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