GENTLE EYES LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops

Gentle Eyes Lubricant Eye Drops by

Drug Labeling and Warnings

Gentle Eyes Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by TRP Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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?

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Monday - Friday.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	03/18/2024

Labeler - TRP Company (105185719)