RITE AID EYE CARE LUBRICANT- carboxymethylcellulose sodium solution/ drops

Rite Aid Eye Care Lubricant by

Drug Labeling and Warnings

Rite Aid Eye Care Lubricant by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. 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 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
• replace cap after using
• do not use if solution chnages color or becomes cloudy

STOP USE

Stop use and ask doctor

• if you experience eye pain, changes in vision, continued redness or irritation of the eye
• if the condition 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 (1-800-222-1222) right away.

INDICATIONS & USAGE

Directions

• Instill 1 or 2 drops in the affected eye(s) as needed.

STORAGE AND HANDLING

Other information

• Use before expiration date marked on container.
• Store at 59° - 86°F (15° - 30°C).
• RETAIN THIS CARTON FOR FUTURE REFERENCE.

INACTIVE INGREDIENT

Inactive ingredients
benzalkonium chloride, boric acid, calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hydroxide

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:
RITE AID
30 HUNTER LANE
CAMP HILL, PA 17011
MADE IN KOREA

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RITE AID EYE CARE LUBRICANT 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-1809
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
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-1809-5	1 in 1 BOX	05/18/2017
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 11822-1809-6	2 in 1 BOX	05/18/2017
2		15 mL in 1 BOTTLE, DROPPER; 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	05/18/2017

Labeler - Rite Aid Corporation (014578892)