QUALITY CHOICE LUBRICANT EYE DROPS HIGH PERFORMANCE- polyethylene glycol 400, propylene glycol solution/ drops 
Chain Drug Marketing Assoc., Inc.

----------

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

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

Purposes

Lubricant

Lubricant

Use

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 feel eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse or lasts more than 72 hours

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

instill 1 or 2 drops in the affected eye(s) as needed

Other information

store at 15º-30ºC (59º-86ºF)

Inactive ingredients

aminomethylpropanol, benzalkonium chloride as preservative, boric acid, hypromellose, potassium chloride, purified water, sodium chloride, sorbitol;

Quality Choice Lubricant Eye Drops High Performance15mL

Quality Choice Lubricant Eye Drops High Performance 15mL

QUALITY CHOICE LUBRICANT EYE DROPS HIGH PERFORMANCE 
polyethylene glycol 400, propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-029
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.4 g  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SORBITOL (UNII: 506T60A25R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
BORIC ACID (UNII: R57ZHV85D4)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-029-151 in 1 BOX12/18/2023
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 DrugM01812/18/2023
Labeler - Chain Drug Marketing Assoc., Inc. (011920774)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(83324-029) , pack(83324-029) , label(83324-029)

Revised: 12/2023
Document Id: 0cd1b36a-a07b-a1db-e063-6294a90a5994
Set id: 0cd1b36a-a07a-a1db-e063-6294a90a5994
Version: 1
Effective Time: 20231218
 
Chain Drug Marketing Assoc., Inc.