Preferred Plus Pharmacy Artificial Tears

Dosage form: solution
Ingredients: POVIDONE, UNSPECIFIED 0.6g in 100mL, POLYVINYL ALCOHOL, UNSPECIFIED 0.5g in 100mL
Labeler: Kinray Inc.
NDC code: 61715-211

Medically reviewed by Drugs.com. Last updated on May 22, 2024.

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	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE, UNSPECIFIED (POVIDONE, UNSPECIFIED)	POVIDONE, UNSPECIFIED	0.6 g in 100 mL
POLYVINYL ALCOHOL, UNSPECIFIED (POLYVINYL ALCOHOL, UNSPECIFIED)	POLYVINYL ALCOHOL, UNSPECIFIED	0.5 g in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM
POTASSIUM CHLORIDE
SODIUM CITRATE
SODIUM PHOSPHATE, DIBASIC
WATER
SODIUM CHLORIDE
SODIUM PHOSPHATE, MONOBASIC
BENZALKONIUM CHLORIDE
DEXTROSE
SODIUM BICARBONATE

Packaging
#	Item Code	Package Description
1	NDC:61715-211-01	1 BOTTLE, DROPPER in 1 CARTON
1		15 mL in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	05/29/2020

Labeler - Kinray Inc. (012574513)

Registrant - K.C. Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Operations
K.C. Pharmaceuticals, Inc.		174450460	manufacture(61715-211), pack(61715-211), label(61715-211)

Revised: 06/2020

Document Id: a6d49bde-a51a-87a6-e053-2a95a90af5f4

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

Version: 2

Effective Time: 20200601

Kinray Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer