QUALITY CHOICE LUBRICANT EYE DROPS RESTORATIVE PERFORMANCE- propylene glycol solution/ drops
Chain Drug Marketing Assoc., Inc.

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Quality Choice Lubricant Eye Drops Restorative Performance 15mL (PLD)

Active ingredient

Propylene glycol 0.6%

Purpose

Lubricant

Use

for the temporary relief of burning and irritation due to dryness of the eye

Warnings

For external use only

Do not use

if this product changes color
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 eye pain
changes in vision occur
redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours

Keep out of reach of children.

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

Inactive ingredients

benzalkonium chloride, boric acid, castor oil, disodium edetate hydrate, **hydrochloric acid, polyoxyethylene sorbitan monooleate, potassium chloride, purified water, sodium borate, sodium chloride, **sodium hydroxide

**May contain these ingredients to adjust pH

Quality Choice Lubricant Eye Drops Restorative Performance 15mL

QUALITY CHOICE LUBRICANT EYE DROPS RESTORATIVE PERFORMANCE
propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:83324-028
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.6 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BORIC ACID (UNII: R57ZHV85D4)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
CASTOR OIL (UNII: D5340Y2I9G)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:83324-028-15	1 in 1 BOX	12/12/2023	05/31/2026
1		15 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	12/12/2023	05/31/2026

Labeler - Chain Drug Marketing Assoc., Inc. (011920774)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Name	Address	ID/FEI	Business Operations
Establishment
Daewoo Pharmaceuticals, Co., Ltd.		689046329	manufacture(83324-028) , pack(83324-028) , label(83324-028)

Revised: 6/2026

Document Id: 5365f2b2-6bc2-4e81-e063-6394a90a64b4

Set id: 0c59876a-50c3-b56c-e063-6394a90a94a8

Version: 3

Effective Time: 20260603

Chain Drug Marketing Assoc., Inc.