REAL- carboxymethylcellulose sodium solution/ drops

Real by

Drug Labeling and Warnings

Real by is a Otc medication manufactured, distributed, or labeled by Oliver Landon Intl Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Uses    

• ▪ For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun
• ▪ May be used as a protectant against further irritation

Warnings

• ▪ For external use only
• ▪ 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
• ▪ If solution changes color or becomes cloudy, do not use

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   

• ▪ Use only if single-use container is intact
• ▪ Use before expiration date marked on container
• ▪ Store at 59°-86°F (15°-33°C)
• ▪ RETAIN THIS CARTON FOR FUTURE REFERENCE

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

PRINCIPAL DISPLAY PANEL

NDC: 59276-403-05

Real
Lubricant
Eye Drops

Moisturizing relief 
Immediate, soothing relief for dry eyes.

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

INGREDIENTS AND APPEARANCE

REAL 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59276-403
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59276-403-05	5 in 1 CARTON	11/14/2018
1		0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2	NDC: 59276-403-30	30 in 1 CARTON	11/14/2018
2		0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	11/14/2018

Labeler - Oliver Landon Intl Inc. (815240195)