WELL AT WALGREENS STERILE LUBRICANT EYE- carboxymethylcellulose sodium solution/ drops 
Walgreens Company

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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Active ingredient                                                                  Purpose

Carboxymethylcellulose Sodium 0.5%.................................. Lubricant

Uses

Warnings

For external use only

Stop use and ask a doctor if you experience eye epain, 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

Directions

Other information

Inactive ingredients

Benzalkonium chloride solution, boric acid, calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, sodium borate, sodium chloride, sodium hydroxide, sterile purified water

Distributed by:

Walgreen Co.

200 Wilmot Rd.

Deerfield, IL 60015

Made in Korea

image description

WELL AT WALGREENS STERILE LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7281
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7281-151 in 1 CARTON
115 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 finalpart34907/20/2015
Labeler - Walgreens Company (008965063)

Revised: 9/2015
Document Id: 6b45e2fb-4ecd-4777-8a30-e0b7ec058535
Set id: 64b5b884-c54c-462d-99a9-b155ef61094c
Version: 3
Effective Time: 20150922
 
Walgreens Company