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

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

Other information

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-259
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.6 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-259-331 in 1 BOX04/01/2024
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01804/01/2024
Labeler - Walmart Inc. (051957769)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Daewoo Pharmaceuticals, Co., Ltd.689046329manufacture(79903-259) , pack(79903-259) , label(79903-259)

Revised: 4/2024
Document Id: 151d54b4-b3fa-92fd-e063-6294a90a2ed2
Set id: 151d54b4-b3f9-92fd-e063-6294a90a2ed2
Version: 1
Effective Time: 20240401
 
Walmart Inc.