Drug Facts

Active ingredient (in each unit dose)

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 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 not 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. 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.

Other Information

Use only if single-use container in intact.
Use before expiration date marked on container.
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Calcium chloride, hydrochloric acid1, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide1, and sodium lactate.

1: May or may not contain this ingredient to adjust pH.

Questions or comments?

800.477.2884, M-F 8 AM – 5 PM Eastern Time

You can also report serious side effects to this number.

PRINCIPAL DISPLAY PANEL - 32 Ampule Carton

NDC 69183-200-32

Eyes
Alive™

Lubricating Eye Drops
Lubricant/carboxymethylcellulose sodium

Long lasting moisturizing
drops to keep your
Eyes Feeling Alive!

IMMEDIATE RELIEF FOR
DRY IRRITATED EYES

32 Sterile Single-Use Containers
0.02 fl oz (0.6 mL) each

MADE IN THE USA

Principal Display Panel - 32 Ampule Carton

EYES ALIVE LUBRICATING
carboxymethylcellulose sodium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69183-200
Route of Administration	INTRAOCULAR

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69183-200-02	2 in 1 POUCH	02/01/2015
1		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
2	NDC:69183-200-04	4 in 1 POUCH	02/01/2015
2		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
3	NDC:69183-200-32	32 in 1 CARTON	02/01/2015
3		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
4	NDC:69183-200-52	52 in 1 CARTON	02/01/2015
4		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
5	NDC:69183-200-72	72 in 1 CARTON	02/01/2015
5		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
6	NDC:69183-200-00	100 in 1 CARTON	02/01/2015
6		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
7	NDC:69183-200-08	8 in 1 CARTON	02/01/2015
7		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part349	02/01/2015

Labeler - DIVISION 5 LABS, INC. (968198288)

Eyes Alive Lubricating