LUBRICATING EYE DROPS- carboxymethylcellulose sodium liquid

LUBRICATING EYE DROPS by

Drug Labeling and Warnings

LUBRICATING EYE DROPS by is a Otc medication manufactured, distributed, or labeled by A2A Integrated Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 of the eye.

Warnings

For external use only

 Do not use if solution changes color or becomes cloudy.

When using this product

to avoid contamination, do no touch tip of container to any surface. Do not reuse. Once open, discard.

Do not touch unit dose tip to eye.

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.

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

Directions

■ TWIST AND REMOVE TAB.

■ Place 1 or 2 drops in the affected eye(s) as needed for relief and discard container.
■ If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions.

Inactive Ingredients

Calcium chloride, hydrochloric acid*, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide*, and sodium
lactate.*May or may not contain this ingredient to adjust pH.

Other information

■ Use only if single-use container is intact.
■ Use before expiration date marked on container.
■ RETAIN THIS FOIL FOR FUTURE REFERENCE.

Principal display panel

INGREDIENTS AND APPEARANCE

LUBRICATING EYE DROPS 
carboxymethylcellulose sodium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73141-001
Route of Administration	OPHTHALMIC

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

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LACTATE (UNII: TU7HW0W0QT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73141-001-01	8 in 1 CARTON	10/04/2019
1		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
2	NDC: 73141-001-02	32 in 1 CARTON	10/04/2019
2		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
3	NDC: 73141-001-03	52 in 1 CARTON	10/04/2019
3		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
4	NDC: 73141-001-04	72 in 1 CARTON	10/04/2019
4		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
5	NDC: 73141-001-05	100 in 1 CARTON	10/04/2019
5		0.6 mL in 1 AMPULE; 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	10/04/2019

Labeler - A2A Integrated Pharmaceuticals, LLC (117064671)