REAL- 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.

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Real Lubricant Eye Drops

Drug Facts

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Use

Warnings

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

If pregnant or breast-feeding, ask a doctor before use.

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 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.

Questions or Comments?

info@oliverlandon.biz

NDC 59276-403-05

Real
Lubricant Eye Drops

Preservative-free

Directions
To open, TWIST AND PULL TAB TO REMOVE

Instill 1 or 2 drops in the affected eye(s) as needed and discard container.
5 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile

580474A2=D640-49CF-B50C-C83420E52E1A-00

REAL 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59276-403
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:59276-403-055 in 1 CARTON11/14/2018
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:59276-403-3030 in 1 CARTON11/14/2018
20.4 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 finalpart34911/14/2018
Labeler - Oliver Landon Intl Inc. (815240195)

Revised: 12/2021
Document Id: b4e02102-512d-4113-e053-2995a90a2efd
Set id: 580474a2-d640-49cf-b50c-c83420e52e1a
Version: 2
Effective Time: 20211205
 
Oliver Landon Intl Inc.