LUBRICANT EYE DROPS- propylene gycol 0.6% solution/ drops
Solis Pharmaceuticals Inc.

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Sterile Lubricant Eye Drops

Active ingredient

Propylene Glycol 0.6%

Purpose

Lubricant

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 exposure to wind or sun
for use as a protectant against further irritation or to relieve dryness of the eye
for use as a lubricant to prevent further irritation or to relieve dryness of the eye

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
do not touch tip of container to any surface to avoid contamination
replace cap after each use

Stop use and ask a doctor if

you experience any of the following:

eye pain,
changes in vision,
continued redness or irritation of the eye,
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 right away.

Directions

shake well before using
Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

store at room temperature
retain carton for future reference

Inactive ingredients

benzalkonium chloride solution, boric acid, calcium chloride, castor oil, disodium edetate, magnesium chloride, polyoxyl 40 hydrogenated castor oil, potassium chloride, purified water, sodium borate, sodium chloride, sodium hyaluronate. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

Label

Single pack

Twin Pack

LUBRICANT EYE DROPS
propylene gycol 0.6% solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:85185-002
Route of Administration	OPHTHALMIC

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

Ingredient Name	Strength
Inactive Ingredients
EDETATE DISODIUM (UNII: 7FLD91C86K)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:85185-002-10	1 in 1 CARTON	03/01/2025	05/31/2026
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC:85185-002-20	2 in 1 CARTON	03/01/2025	05/31/2026
2		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	03/01/2021	05/31/2026

Labeler - Solis Pharmaceuticals Inc. (119380963)

Name	Address	ID/FEI	Business Operations
Establishment
Daewoo Pharmaceuticals		689046329	manufacture(85185-002)

Revised: 6/2026

Document Id: 5366c3b0-8ff2-02b5-e063-6294a90aa0ca

Set id: 30887786-70fe-4768-e063-6394a90a5a38

Version: 4

Effective Time: 20260604

Solis Pharmaceuticals Inc.