WELL LUBRICANT EYE DROPS- propylene glycol liquid

Well Lubricant Eye Drops by

Drug Labeling and Warnings

Well Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by True Marker Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (s)                      Purpose

Propylene Glycol 0.7%                    Lubricant

PURPOSE

Uses

• for the temporary relief of burning and irritation due to dryness of the eye
• for the temporary relief of discomfort due to minor irritations of the eye or to exposureto wind or sun

Warnings

For external use only

Do not use

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

When using this product

• to avoid contamination do no touch tip of container to any surface 
• replace cap after each use 
• remove contact lenses before use

Stop use and ask a doctor if you experience any of the
following:

• eye pain 
• change in vision
• continued redness or irritation of the eye
• condition worsens or persisters for more than 72 hours

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

KEEP OUT OF REACH OF CHILDREN

Directions

• Shake well before using. 
• Put 1 or 2 drops in the affected eye (s) as needed.

Other information

store at 15°-30°C (59°-86°F)

Inactive Ingredients

Water, Boric Acid, Potassium Chloride, Sorbitol, Glycerin, Hyluronic Acid, Amynomethylpropanol, Benzalhonium Chloride, Sodium Chorlide, Hydrochloric Acid, Sodium Hydroxide

Questions?

1-888-811-2634.

Product label

INGREDIENTS AND APPEARANCE

WELL LUBRICANT EYE DROPS 
propylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83592-040
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.7 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONIC ACID (UNII: S270N0TRQY)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83592-040-01	5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/26/2024
2	NDC: 83592-040-02	2 in 1 CARTON	08/26/2024
2		5 mL in 1 BOTTLE, PLASTIC; 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	08/26/2024

Labeler - True Marker Pharmaceuticals, Inc. (119046582)