LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops 
Oliver Landon Intl Inc.

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.

----------

Lubricant Eye Drops

Drug Facts

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Uses

Warnings

For external use only

Do not use if solution changes color or becomes cloudy

When using this product

  • do not touch tip of container to any surface to avoid contamination.
  • do not reuse. Once opened, discard.

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness or irritation of the eye
  • condition 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

*If used for post-operative dryness and discomfort, follow your eye doctor’s instructions.

Other information

RETAIN THIS CARD FOR FUTURE REFERENCE.

Use only if single-use container is intact.

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.

Questions & Comments? 1 (800) 839-5929

Manufactured for: Oliver Landon Intl. Inc.

The Grove, 21 Pine Road

Belleville, St. Michael, BARBADOS BB11113

Lubricant Eye Drops
0.4 ml (0.014 fl oz) per vial

Lubricant Eye Drops vial label

LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59276-905
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
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59276-905-055 in 1 CELLO PACK02/25/2019
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 finalpart34902/25/2019
Labeler - Oliver Landon Intl Inc. (815240195)

Revised: 11/2020
Document Id: b4e07cf0-5f4c-bcaf-e053-2995a90aee25
Set id: ec3160ac-a2d1-4132-a75a-4180b4bafdf3
Version: 2
Effective Time: 20201124
 
Oliver Landon Intl Inc.