EQUATE RESTORE PLUS LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops 
Walmart, Inc.

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Equate Restore Plus 70 Ct. (PLD)

Active ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

Carboxymethylcellulose sodium.....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 chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate. **May contain these ingredients to adjust pH.

Questions or comments? Call 1-888-287-1915

Equate Restore Plus Lubricant Eye Drops 70ct

Equate Restore Plus Lubricant Eye Drops 70ct

EQUATE RESTORE PLUS LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-389
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
SODIUM LACTATE (UNII: TU7HW0W0QT)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-389-0170 in 1 CARTON03/04/2022
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 DrugM01803/04/2020
Labeler - Walmart, Inc. (051957769)
Registrant - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
K.C. Pharmaceuticals, Inc.174450460pack(49035-389) , label(49035-389)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052manufacture(49035-389)

Revised: 12/2023
Document Id: 0d2940ee-e127-56cc-e063-6394a90aaa51
Set id: 9e665ca2-4fa6-fdb4-e053-2a95a90abcca
Version: 7
Effective Time: 20231223
 
Walmart, Inc.