FDA.reportPublic FDA data

Medi-First Lubricant Eye Drops

Manufacturer
Unifirst First Aid Corporation | KC Pharmaceuticals, Inc. | Unimed Pharmaceuticals, Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:29:40

Label at a glance#

ProductMedi-First Lubricant Eye Drops
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun for use a protectant against further irritation

Dosage and administration

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 your eye doctor's instructions

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose sodium 0.5%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use

  • 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 - STOP USE SECTION

Stop use and aska 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 od reach of children.

If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 your eye doctor's instructions

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

** May contain these ingredients to adjust pH

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-634-7680

Medi-First Lubricant Eye Drops Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 47682-193-83

*Compare to the active ingredient in Refresh Plus®

Medi-First®

Preservative-free

Lubricant Eye Drops

Carboxymethylcellulose Sodium 0.5%

Eye Lubricant

Immediate, long-lasting relief for dry, irritated eyes

Sterile

30 Single-Use Containers

0.01 fl oz (0.4 mL) each

MF LubricantMF Lubricant

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionPSN7
1188426carboxymethylcellulose sodium 5 MG/ML Ophthalmic SolutionSCD7
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionSY7
1188426carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic SolutionSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-193-83Medi-First Lubricant Eye Drops30 in 1 BOXSOLUTION307
47682-193-83Medi-First Lubricant Eye Drops0.4 mL in 1 AMPULESOLUTION0.47

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-19347682-193-83

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
SODIUM LACTATETU7HW0W0QTIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
HYDROCHLORIC ACIDQTT17582CBIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
POTASSIUM CHLORIDE660YQ98I10IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311ACTIB

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
Medi-First Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMUnifirst First Aid Corporationa4e651cc-adf0-af9e-e053-2995a90ace5a2025-12-30WarningsExact identifier
ndc (package): 47682-193-83
ndc (product): 47682-193
ndc11 (package): 47682019383
spl id: 4735597f-6299-c349-e063-6294a90a09ec
spl set id: a4e651cc-adf0-af9e-e053-2995a90ace5a

Reported adverse events (FAERS/openFDA)#

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