RESTORE PLUS SINGLE VIAL- carboxmethylcellulose sodium solution/ drops

Restore Plus Single Vial by

Drug Labeling and Warnings

Restore Plus Single Vial by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

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

PURPOSE

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

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 eyes.
• if solution changes color or becomes cloudy, do not use

STOP USE

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

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

INDICATIONS & USAGE

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

STORAGE AND HANDLING

Other information

• use only if single-use container is intact
• use before expiration date marked on container
• store at 59°-86°F (15°-30°C)
• retain carton for future reference

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

Distributed by:

Wal-Mart Stores, Inc.

Bentonville, AR 72716

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RESTORE PLUS SINGLE VIAL 
carboxmethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-657
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
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-657-04	0.4 mL in 1 VIAL; Type 0: Not a Combination Product	01/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/01/2016

Labeler - United Exchange Corp. (840130579)

Registrant - United Exchange Corp. (840130579)