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

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Equate Complete Relief Lubricant Eye Drops 15mL (PLD)

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

Equate Complete Relief Lub Eye Drops 15mL

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

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79903-259-33	1 in 1 BOX	04/01/2024	05/31/2026
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	04/01/2024	05/31/2026

Labeler - Walmart Inc. (051957769)

Registrant - KC Pharmaceuticals, Inc. (174450460)

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

Revised: 6/2026

Document Id: 53661586-e0ef-6e23-e063-6394a90a595c

Set id: 151d54b4-b3f9-92fd-e063-6294a90a2ed2

Version: 3

Effective Time: 20260603

Walmart Inc.