EQUATE LUBRICANT EYE DROPS- polyethylene glycol 400, propylene glycol solution/ drops 
Walmart, Inc.

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Equate Lubricant Eye Drops 30ct (PLD)

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

Purpose

Lubricant

Lubricant

Use

Warnings

For external use only

Do not use

  • if this solution 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
  • do not reuse. Once opened, discard.

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse or lasts more than 72 hours

If pregnant or breast-feeding,

ask a health professional before use.

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

boric acid, hypromellose, potassium chloride, purified water, sodium chloride.

May contain sodium hydroxide and/or hydrochloric acid to adjust pH.

Equate Lubricant Eye Drops 30ct

Equate Lubricant Eye Drops 30ct

EQUATE LUBRICANT EYE DROPS 
polyethylene glycol 400, propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-131
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.4 g  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-131-3030 in 1 BOX07/20/2022
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01807/20/2022
Labeler - Walmart, Inc. (051957769)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Unimed689852052manufacture(79903-131) , pack(79903-131) , label(79903-131)

Revised: 12/2023
Document Id: 0d383700-e255-881f-e063-6294a90a347c
Set id: deebaf7f-f20d-4d7f-e053-2a95a90a4b4f
Version: 4
Effective Time: 20231223
 
Walmart, Inc.