EQUATE MOISTURIZING COMFORT LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops

Equate Moisturizing Comfort Lubricant Eye Drops by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

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 external use only

Do not use

• if this product changes color or becomes cloudy
• if you are sensitive to any ingredient in this product

When using this product

• to avoid contamination, do not touch tip of container to any surface. Replace cap after using.

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

instill 1 to 2 drops in the affected eye(s) as needed

Other information

store at 15-25°C (59-77°F)

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride hydrate (dihydrate), **hydrochloric acid, magnesium chloride, potassium chloride, sodium borate, sodium chloride, **sodium hydroxide, water for injection

**May contain these ingredients to adjust pH

Questions or comments?

Call 1-888-287-1915

Equate Moisturizing Comfort Lubricant Eye Drops 15mL

INGREDIENTS AND APPEARANCE

EQUATE MOISTURIZING COMFORT LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-264
Route of Administration	OPHTHALMIC

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

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CALCIUM CHLORIDE MONOHYDRATE (UNII: LEV48803S9)
HYDROCHLORIC ACID (UNII: QTT17582CB)
BORIC ACID (UNII: R57ZHV85D4)
SODIUM BORATE (UNII: 91MBZ8H3QO)
WATER (UNII: 059QF0KO0R)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-264-05	1 in 1 BOX	04/01/2024
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	04/01/2024

Labeler - Walmart Inc. (051957769)

Registrant - KC Pharmaceuticals, Inc. (174450460)