LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops

Lubricant Eye Drops by

Drug Labeling and Warnings

Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by KC Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Carboxymethylcellulose sodium 0.5%

PURPOSE

Eye Lubricant

INDICATIONS & USAGE

• 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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

• To open, pull and twist tab to remove

• Instill 1 or 2 drops in the affected eye(s) as needed and discard container

INACTIVE INGREDIENT

Calcium Chloride, **Hydrochloric acid, Magnesium Chloride, Potassium Chloride, Purified water, Sodium Chloride, **Sodium Hydroxide, Sodium Lactate. **May contain these ingredients to adjust pH.

WARNINGS

Warnings

For external use only

Do not use this product 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 to eye

Stop use and ask a doctor if you experience any of the following

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye continues
• redness or irritation of the eye gets worse or lasts more than 72 hours

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55651-510
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
WATER (UNII: 059QF0KO0R)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LACTATE (UNII: TU7HW0W0QT)
HYDROCHLORIC ACID (UNII: QTT17582CB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55651-510-01	5 in 1 BOX	02/25/2026
1		0.4 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	02/25/2026

Labeler - KC Pharmaceuticals, Inc. (174450460)