Preferred Plus Pharmacy Artificial Tears (PLD)

Preferred Plus Pharmacy Artificial Tears by

Drug Labeling and Warnings

Preferred Plus Pharmacy Artificial Tears by is a Otc medication manufactured, distributed, or labeled by Kinray Inc., K.C. Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PREFERRED PLUS PHARMACY ARTIFICIAL TEARS- polyvinyl alcohol, povidone solution 
Kinray

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Preferred Plus Pharmacy Artificial Tears (PLD)

Active ingredients

Polyvinyl alcohol.....0.5%

Povidone.....0.6%

Purpose

Polyvinyl alcohol....Eye lubricant

Povidone....Eye lubricant

Uses

• for use as a protectant against further irritation or to relieve dryness of the eye
• for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun

Warnings

For external use only

• Do not use this product if solution changes color or becomes cloudy

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

When using this product

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

Keep out of the reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

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

Inactive ingredients

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

Other information

• Tamper Evident. Do not use this product if imprinted neckband is missing or broken.
• RETAIN THIS CARTON FOR FUTURE REFERENCE
• Store at 15º-30ºC (58º-86ºF)

PREFERRED PLUS PHARMACY ARTIFICIAL TEARS 
polyvinyl alcohol, povidone solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61715-211
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990)	POLYVINYL ALCOHOL, UNSPECIFIED	0.5 g  in 100 mL
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E)	POVIDONE, UNSPECIFIED	0.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61715-211-01	1 in 1 CARTON	05/29/2020	06/30/2022
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	05/29/2020	06/30/2022

Labeler - Kinray (012574513)

Revised: 5/2025

Document Id: 2ee65247-3916-40f6-ae5d-e1d59cf60c6f

34390-5

Set id: 9e8421bd-dde8-322d-e053-2995a90ab7bf

Version: 4

Effective Time: 20250530