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

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Quality Choice Lubricant Eye Drops Long Lasting 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-86°F)

Inactive ingredients

benzalkonium chloride as preservative, boric acid, calcium chloride, hypromellose, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, zinc chloride

Quality Choice Lubricant Eye Drops Long Lasting 15mL

Quality Choice Lubricant Eye Drops Long Lasting 15mL

QUALITY CHOICE LUBRICANT EYE DROPS LONG LASTING 
polyethylene glycol 400, propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-030
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
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
BORIC ACID (UNII: R57ZHV85D4)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
ZINC CHLORIDE (UNII: 86Q357L16B)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-030-151 in 1 BOX12/19/2023
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 DrugM01812/19/2023
Labeler - Chain Drug Marketing Assoc., Inc. (011920774)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460pack(83324-030) , manufacture(83324-030) , label(83324-030)

Revised: 12/2023
Document Id: 0cd91c45-88a3-f88c-e063-6294a90ad127
Set id: 0cd91c45-88a2-f88c-e063-6294a90ad127
Version: 1
Effective Time: 20231219
 
Chain Drug Marketing Assoc., Inc.