WALGREENS ULTRA LUBRICANT- polyethylene glycol 400, and propylene glycol solution/ drops

Walgreens Ultra Lubricant by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose

Polyethylene Glycol 400 0.4%...........................Eye lubricant

Propylene Glycol 0.3%......................................Eye lubricant

PURPOSE

Uses

• for the temporary relief of burning and irritation due to:
• dryness of the eyes
• exposure to wind or sun

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

• if this product changes color or becomes cloudy
• if you are sensitive to any ingredient in this product

WHEN USING

When using this product

• remove contact lenses before using
• replace cap after each use
• do not touch tip of bottle to any surface to avoid contamination

STOP USE

Stop use and ask a doctor if

• you experience eye pain and/or vision change
• you continue to have eye redness and/or irritation
• irritation, burning persists or worsens for more than 72 hours

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

• shake well before using
• instill 1 or 2 drops in the affected eye(s) as needed
• children under 6 years of age: ask a doctor

STORAGE AND HANDLING

Other information

• store at room temperature

INACTIVE INGREDIENT

Inactive ingredients

boric acid, calcium chloride, chlorhexidine gluconate, hydrochloric acid, hypromellose 2910 (4000 mpa.s), magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hdyroxide, zinc chloride

DOSAGE & ADMINISTRATION

Distributed by:

Walgreen Co.

Deerfield, IL 60015

Made in South Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS ULTRA LUBRICANT 
polyethylene glycol 400, and propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-6154
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	4 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
ZINC CHLORIDE (UNII: 86Q357L16B)
HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)
WATER (UNII: 059QF0KO0R)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-6154-05	1 in 1 CARTON	08/29/2025
1		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 Drug	M018	08/29/2025

Labeler - Walgreens (008965063)