Drug Labeling and Warnings

Drug Details [pdf]

LUBRICANT EYE DROPS HIGH PERFORMANCE- polyethylene glycol, propylene glycol liquid 
KC Pharmaceuticals, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredients

Polyethylene glycol 400  0.4%
Propylene glycol   0.3%

Purpose

Polyethylene glycol 400............. Lubricant
Propylene glycol............ Lubricant

Uses
for the temporary relief of burning and irritation due to dryness of the eye

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 the 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

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Centerright away.

Directions
Instill 1 or 2 drops in the affected eye(s) as needed
Children under 6 years of age: ask a doctor

Other information

• RETAIN THIS CARTON FOR FUTURE REFERENCE
• Store at room temperature

Inactive ingredients

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

LUBRICANT EYE DROPS HIGH PERFORMANCE 
polyethylene glycol, propylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55651-101
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	0.4 g  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
HYPROMELLOSES (UNII: 3NXW29V3WO)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55651-101-01	1 in 1 BOX	02/11/2019
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 final	part349	02/11/2019

Labeler - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
KC Pharmaceuticals, Inc.		174450460	manufacture(55651-101) , pack(55651-101) , label(55651-101)

Revised: 3/2019

Document Id: ac71259f-acbe-436c-a908-6717df110095

34390-5

Set id: 8056e4fd-11b3-46f0-bd69-7bcc8978ed24

Version: 1

Effective Time: 20190327