EQUATE LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops

Equate Lubricant Eye Drops by

Drug Labeling and Warnings

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

Drug Details [pdf]

PURPOSE

Purpose: Lubricant

DOSAGE & ADMINISTRATION

Directions:
instill 1 to2 drops in the affected eye(s) as needed

WARNINGS

Warnings
For external use only
Do not use
■ If thisproduct 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 to 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(1-800-222-1222) right away.

ACTIVE INGREDIENT

Active ingredient
Carboxymethylcellulose sodium 0.5%.

INDICATIONS & USAGE

Uses
■ for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun
■ maybe used as a protectant against further irritation

INACTIVE INGREDIENT

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 hydrochloric acid and sodium hydroxide to adjust pH

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11716-0364
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 mg  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11716-0364-5	1 in 1 BOX	12/26/2025
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	12/26/2025

Labeler - Hanlim (687986034)