EZRICARE Artificial Tears Lubricant Eye Drops

ARTIFICIAL TEARS LUBRICANT EYE DROPS by

Drug Labeling and Warnings

ARTIFICIAL TEARS LUBRICANT EYE DROPS by is a Otc medication manufactured, distributed, or labeled by Ezricare Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ARTIFICIAL TEARS LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops 
Ezricare Llc

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EZRICARE Artificial Tears Lubricant Eye Drops

Drug Facts

Active Ingredient

Carboxymethylcellulose Sodium 10 MG in 1 ml.

Purpose

Eye Lubricant

Uses

for use as a protectant against further irritation or to relieve dryness of the eye

for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun

Warnings

For external use only

Do not use this product if solution changes color or becomes cloudy

Stop use and ask a doctor if you experience

eye pain  changes in vision

continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours

When using this product

to avoid contamination do not touch tip of container to any surface  replace cap after using. Keep container tightly closed.

remove contact lens before using

Keep out of the reach children. If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Questions or comments?

718-502-6610

between 9 am and 4 pm EST, Monday - Friday.

Directions

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Tamper Evident. Do not use this product if neckband is missing or broken.

RETAIN THIS CARTON FOR FUTURE REFERENCE

Store at 15°-30°C (59°-86°F)

Inactive Ingredients

Boric Acid

Potassium Chloride

Sodium Chloride

Calcium Chloride Dihydrate.

Magnesium Chloride

Sodium Chlorite

Sodium Hydroxide and 

Water for Injection

Compare to the active Ingredient in Refresh Plus Eye Drops

Refresh, Lubricate and Moisturizes

Distributed by.

EzriCare, LLC

Lakewood, NJ

www.EzriCare.com

Packaging

ARTIFICIAL TEARS LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79503-101
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SODIUM CHLORITE (UNII: G538EBV4VF)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79503-101-15	1 in 1 CARTON	11/22/2020	02/02/2023
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	11/22/2020	02/02/2023

Labeler - Ezricare Llc (117573818)

Revised: 1/2024

Document Id: 35576ab9-9ec7-42bf-83a9-5f5d6d0c5c1c

34390-5

Set id: ac1ea23c-f1c6-418f-921e-58553ee919cb

Version: 3

Effective Time: 20240118

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