Drug Facts

Active Ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

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

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

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

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

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-193
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM	0.5 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-193-83	30 in 1 BOX	09/01/2020
1		0.4 mL in 1 AMPULE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	09/01/2020

Labeler - Unifirst First Aid Corporation (832947092)

Name	Address	ID/FEI	Business Operations
Establishment
Unimed Pharmaceuticals, Inc.		689852052	pack(47682-193) , manufacture(47682-193) , label(47682-193)

Medi-First Lubricant Eye Drops (PLD)