LUBRICANT EYE- carboxymethylcellulose sodium solution/ drops 
The Kroger Co.

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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Kroger Lubricant Eye Drops

Active ingredient
Carboxymethylcellulose sodium 0.5%

Purpose
Carboxymethylcellulose sodium.............Eye Lubricant

Uses

​Warnings

For external use only.

Do not use if solution changes color or becomes cloudy.

When using the product to avoid contamination

  • do not touch tip of container to any surface.
  • do not reuse.
  • once opened, discard.
  • 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 reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Other information

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

Questions or comments?
1-800-632-6900

Carton

LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-373
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
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-373-3330 in 1 BOX06/01/2015
10.5 mL in 1 VIAL, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34906/01/2015
Labeler - The Kroger Co. (006999528)
Registrant - Unimed Pharmaceuticals, Inc. (689852052)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052label(30142-373) , manufacture(30142-373) , pack(30142-373)

Revised: 12/2019
Document Id: 98efd794-6c23-b100-e053-2a95a90a9f0c
Set id: 046f4ebc-d8f9-4755-b6ba-790fe86f3128
Version: 4
Effective Time: 20191205
 
The Kroger Co.