Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
May be used as a protectant against further irritation.

Warnings

For use in eyes only.
Retain outer carton for full product drug facts.

Stop use and ask a doctor if:

You experience eye pain, changes in vision, continued redness or irritation of the eye.
The condition worsens or persists for more than 72 hours.

Keep out of reach of children.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right awav.

Do not use

• If solution changes color or becomes cloudy.

When using this product:

Avoid contamination, do not touch tip of container to any surface.
Replace cap after use.

If pregnant or breast feeding

If pregnant or breast feeding, ask a health professional before use.

Directions

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

Other information

Store at room temperature 15°-30°C (59°-86°F).
Keep tightly closed.
EXPIRATION DATE ONLY REFERS TO THE UNOPENED BOTTLE.
The use of this container by more than one person may spread infection.

Inactive ingredients

Boric acid, Calcium| chloride, Hydrochloric acid*, Magnesium chloride, Potassium chloride, Purified water, Sodium borate, Sodium chloride, Sodium hydroxide*. Stabilized axychloro complex 2.5%.

*May contain one or more of these ingredients to adjust pH.

Questions or comments?

1-888-969-6855

8 am to 4 pm EST;

Monday - Friday.

PRINCIPAL DISPLAY PANEL

Carton

Label

GENTLE EYES LUBRICANT EYE DROPS
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:17312-430
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORITE (UNII: G538EBV4VF)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:17312-430-15	1 in 1 CARTON	03/18/2024
1		15 mL in 1 BOTTLE, DROPPER; 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	03/18/2024

Labeler - TRP Company (105185719)

Gentle Eyes Lubricant Eye Drops™