RESTORE PLUS SINGLE VIAL- carboxmethylcellulose sodium solution/ drops 
United Exchange Corp.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Refresh Plus Single Vial Eye Drops 0.4 ml Bulk 6577ZZ (2018)

Active ingredient Purpose

Carboxymethylcellulose sodium 0.5%.........................Eye lubricant

Uses

Warnings

For external use only.

Stop use and ask a doctor if you experience eye pain changes in vision, continued redness or irritation of the eye, or in the condtion worsens or persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

To open, twist and pull tab to remove. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

if used for post-operative (e.g. LASIK) dryness and discomfort, follow your eye doctor's instructions

Other information

Inactive ingredients calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, and sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH

Distributed by:

Wal-Mart Stores, Inc.

Bentonville, AR 72716

Made in Korea

single

RESTORE PLUS SINGLE VIAL 
carboxmethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-657
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM LACTATE (UNII: TU7HW0W0QT)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-657-040.4 mL in 1 VIAL; Type 0: Not a Combination Product01/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/01/2016
Labeler - United Exchange Corp. (840130579)
Registrant - United Exchange Corp. (840130579)

Revised: 11/2021
Document Id: d0796e76-bb55-8b56-e053-2a95a90a53b2
Set id: 63658c76-de87-c04e-e053-2a91aa0ac711
Version: 2
Effective Time: 20211110
 
United Exchange Corp.