WALGREENS LUBRICANT EYE- carboxymethylcellulose sodium solution/ drops

Walgreens Lubricant Eye by

Drug Labeling and Warnings

Walgreens Lubricant Eye by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Walgreens Lubricant Eye Drops

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 or exposure to wind or sun

may be used as a protectant against further irritation.

Warnings

 For use in the eyes only. 

Retain outer carton for full product drug facts.

Do not use

if solution changes color or becomes cloudy.

When using this product

avoid contamination, do not touch tip of container to any surface. 

replace cap after use.

Stop use and ask a doctor if

you experience eye pain, changes in vision, continued redness or irritation of the eye.

the condition worsens or persists for more than 72 hours.

Keep this and all drugs out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

 Shake well before use.

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

store at room temperature 15°-30°C (59°-86°F)

keep tightly closed

Inactive ingredients

Boric acid, calcium chloride, magnesium chloride, potassium chloride, sodium borate, sodium chloride, water for injection. Vanish® (Stabilized Peroxycomplex System as a preservative). May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions?

1-800-925-4733 Monday thru Friday 8:30am - 5:00pm EST

PRINCIPAL DISPLAY PANEL

Walgreens
NDC: 0363-0185-13
Lubricant
Eye Drops
MOISTURIZING
0.5 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL

Walgreens
NDC: 0363-0185-49
Lubricant
Eye Drops
MOISTURIZING
2 BOTTLES 
0.5 FL OZ (15 mL) EACH
1.0 FL OZ (30ML) TOTAL

INGREDIENTS AND APPEARANCE

WALGREENS LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0185
Route of Administration	OPHTHALMIC

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

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0185-13	1 in 1 CARTON	04/01/2019
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 0363-0185-49	2 in 1 CARTON	04/01/2019
2		15 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	04/01/2019

Labeler - Walgreen Company (008965063)