EYES ALIVE EYECON LUBRICATING- carboxymethylcellulose sodium, unspecified form liquid 
DIVISION 5 LABS, INC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Eyes Alive EYECON
Lubricating

Drug Facts

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Uses

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

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

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton
EYES ALIVE EYECON  LUBRICATING
carboxymethylcellulose sodium, unspecified form liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69183-205
Route of AdministrationINTRAOCULAR
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69183-205-011 in 1 CARTON01/07/2019
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:69183-205-022 in 1 CARTON01/07/2019
210 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/07/2019
Labeler - DIVISION 5 LABS, INC. (968198288)

Revised: 11/2019
Document Id: feff818b-dee3-4f8a-843c-32364ac3215e
Set id: 7b0b0386-e4ba-43f8-9e2f-c3eb43f45643
Version: 2
Effective Time: 20191119
 
DIVISION 5 LABS, INC.