EYES ALIVE EYECON LUBRICATING- carboxymethylcellulose sodium, unspecified form liquid

Eyes Alive EYECON by

Drug Labeling and Warnings

Eyes Alive EYECON by is a Otc medication manufactured, distributed, or labeled by DIVISION 5 LABS, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

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.
• 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 to any surface
• replace cap after using

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or 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 (1-800-222-1222) right away

Directions

Place 1 to 2 drops in the affected eye(s) as needed

Other Information

• use before expiration date marked on container
• store at room temperature
• remove contact lenses before using
• 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?

1-800 477-2884 M-F 8 AM 5 PM Eastern Time

You can also report serious side effects to this number.

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton

NDC 69183 205 01

Eyes
Alive™

EYECON™
LUBRICATING EYE DROPS
MULTI DOSE

FOR
DRY EYE
RELIEF

MAKE YOUR
EYES FEEL
Alive
AGAIN

USE AS
OFTEN AS
NEEDED

PRESERVATIVE FREE

STERILE
0.3 FL OZ (10 mL)

Over
240
Drops

MADE IN USA

INGREDIENTS AND APPEARANCE

EYES ALIVE EYECON  LUBRICATING
carboxymethylcellulose sodium, unspecified form liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69183-205
Route of Administration	INTRAOCULAR

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: 69183-205-01	1 in 1 CARTON	01/07/2019
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 69183-205-02	2 in 1 CARTON	01/07/2019
2		10 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	01/07/2019

Labeler - DIVISION 5 LABS, INC. (968198288)