QUALITY CHOICE ARTIFICIAL TEARS LUBRICANT EYE DROPS- polyvinyl alcohol, povidone solution/ drops 
Chain Drug Marketing Association, Inc.

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Quality Choice Artificial Tears15 mL (PLD)

Active Ingredients

Polyvinyl alcohol 0.5%

Povidone 0.6%

Purpose

Lubricant

Lubricant

Uses

Warnings

For external use only

Do not use this product if

  • solution changes color or becomes cloudy

When using this product

  • remove contact lens before using
  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using. Keep container tightly closed

Stop use and ask a doctor if you experience

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours

Keep out of the reach of children.

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

Directions

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

Other information

Inactive ingredients

benzalkonium chloride, dextrose, edetate disodium, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate dibasic, and sodium phosphate monobasic

Quality Choice Artificial Tears Lubricant Eye Drops 15mL

Quality Choice Artificial Tears Lubricant Eye Drops 15mL

QUALITY CHOICE ARTIFICIAL TEARS LUBRICANT EYE DROPS 
polyvinyl alcohol, povidone solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-189
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL (UNII: 532B59J990) (POLYVINYL ALCOHOL - UNII:532B59J990) POLYVINYL ALCOHOL0.5 g  in 100 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE0.6 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
DEXTROSE (UNII: IY9XDZ35W2)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-189-141 in 1 BOX08/11/2024
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 DrugM01808/11/2024
Labeler - Chain Drug Marketing Association, Inc. (011920774)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(83324-189) , label(83324-189) , pack(83324-189)

Revised: 8/2024
Document Id: 1f663002-c5f8-51be-e063-6394a90a997f
Set id: 1f669655-4bc7-0175-e063-6294a90a305a
Version: 1
Effective Time: 20240811
 
Chain Drug Marketing Association, Inc.