MEDI-FIRST LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution 
Unifirst First Aid Corporation

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Medi-First Lubricant Eye Drops

Drug Facts

Active Ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

Warnings

For external use only

Do not use

  • if solution changes color or becomes cloudy

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

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

Keep out od reach of children.

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

Directions

Other information

Inactive ingredients

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?

Call 1-800-634-7680

Medi-First Lubricant Eye Drops Label

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 Lubricant

MEDI-FIRST LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-193
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM LACTATE (UNII: TU7HW0W0QT)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-193-8330 in 1 BOX09/01/2020
10.4 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01809/01/2020
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 1/2024
Document Id: 0f17236c-a153-a1eb-e063-6294a90ab7db
Set id: a4e651cc-adf0-af9e-e053-2995a90ace5a
Version: 4
Effective Time: 20240116
 
Unifirst First Aid Corporation