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

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

Other information

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 15mL

QUALITY CHOICE LUBRICANT EYE DROPS RESTORATIVE PERFORMANCE 
propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-028
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.6 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
CASTOR OIL (UNII: D5340Y2I9G)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-028-151 in 1 BOX12/12/2023
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01812/12/2023
Labeler - Chain Drug Marketing Assoc., Inc. (011920774)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Daewoo Pharmaceuticals, Co., Ltd.689046329manufacture(83324-028) , pack(83324-028) , label(83324-028)

Revised: 12/2023
Document Id: 0c59876a-50c4-b56c-e063-6394a90a94a8
Set id: 0c59876a-50c3-b56c-e063-6394a90a94a8
Version: 1
Effective Time: 20231212
 
Chain Drug Marketing Assoc., Inc.