EQUATE COMPLETE RELIEF LUBRICANT EYE DROPS- propylene glycol solution/ drops

Equate Complete Relief Lubricant Eye Drops by

Drug Labeling and Warnings

Equate Complete Relief Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Walmart Inc., KC Pharmaceuticals, Inc., Daewoo Pharmaceuticals, Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Propylene glycol 0.6%

Purpose

Lubricant

Use

• for the temporary relief of burning and irritation due to dryness of the eye

Warnings

For external use only

Do not use

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

When using this product

• do not touch tip of container to any surface to avoid contamination
• repace cap after each use

Stop use and ask a doctor if

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye(s) gets worse, persists or lasts 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

• shake well before using
• instill 1 or 2 drops in the affected eye(s) as needed

Other information

• store at 59-77°F (15-25°C)

Inactive ingredients

benzalkonium chloride, boric acid, castor oil, disodium edetate hydrate, **hydrochloric acid, polyoxyethylene sorbitan monooleate, potassium chloride, purified water, sodium borate, sodium chloride, **sodium hydroxide

**May contain these ingredients to adjust pH.

Questions or comments?

Call 1-888-287-1915

Equate Complete Relief Lubricant Eye Drops 15mL

INGREDIENTS AND APPEARANCE

EQUATE COMPLETE RELIEF LUBRICANT EYE DROPS 
propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-259
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
BORIC ACID (UNII: R57ZHV85D4)
CASTOR OIL (UNII: D5340Y2I9G)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROCHLORIC ACID (UNII: QTT17582CB)
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-259-33	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)

Establishment
Name	Address	ID/FEI	Business Operations
Daewoo Pharmaceuticals, Co., Ltd.		689046329	manufacture(79903-259) , pack(79903-259) , label(79903-259)