EQUATE LUBRICANT EYE DROPS PRESERVATIVE-FREE- carboxymethylcellulose sodium solution/ drops 
Wal-Mart Stores, Inc.

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Equate Lubricant Eye Drops Preservative-Free (PLD)

Active ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

Lubricant

Uses

Warnings

For external use only

Do not use this product if

  • solution changes color or becomes cloudy

When using this product

  • do not reuse
  • once opened, discard
  • to avoid contamination, do not touch tip of container to any surface
  • do not touch unit-dose tip to eye

Stop use and ask a doctor if

  • you experience eye pain
  • changes in vision occur
  • redness or irritation of the eye continues
  • redness or irritation of the eye worsens or persists for more than 72 hours

Keep out of the reach of children.

If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

Other information

Inactive ingredients

calcium chloride, **hydrochloric acid, magnesium choride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.

**May contain these ingredients to adjust pH.

Questions or comments?

1-888-287-1915

Equate Preservative-Free Lubricant Eye Drops 25ct

Equate Lubricant Eye Drops 25ct

EQUATE LUBRICANT EYE DROPS PRESERVATIVE-FREE 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-245
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYDROCHLORIC ACID (UNII: QTT17582CB)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-245-0125 in 1 BOX11/01/2019
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 DrugM01811/01/2019
Labeler - Wal-Mart Stores, Inc. (051957769)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460pack(49035-245) , label(49035-245)
Establishment
NameAddressID/FEIBusiness Operations
Unimed689852052manufacture(49035-245)

Revised: 12/2023
Document Id: 0d293bad-388b-0566-e063-6294a90ad581
Set id: 9228a39b-38d2-1dfc-e053-2a95a90a3c90
Version: 4
Effective Time: 20231223
 
Wal-Mart Stores, Inc.