Lubricant Eye Drop by Innovida Pharmaeutique Corporation

Lubricant Eye Drop by

Drug Labeling and Warnings

Lubricant Eye Drop by is a Otc medication manufactured, distributed, or labeled by Innovida Pharmaeutique Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LUBRICANT EYE DROP- propylene glycol liquid 
Innovida Pharmaeutique Corporation

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Active Ingredient

Propylene Glycol 0.6%

Purpose

Lubricant

Uses

• for the temporary relief of burning and irritation due to 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 

• 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
• remove contact lenses before use

Stop use and ask a doctor if you experience any of the following:

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

Keep out of reach of children

If swallowed, get medical help or contact Poison Control Center right away.

Directions

Shake well before using. Put 1 or 2 drops in the affected eye (s) as needed

Other information

store at room temperature

Inactive Ingredients

Water, Boric Acid, Potassium Chloride, Sorbitol, Glycerin, Hyluronic Acid, Amynomethylpropanol, Benzalhonium Chloride, Sodium Chorlide, Hydrochloric Acid, Sodium Hydroxide

Product label

LUBRICANT EYE DROP 
propylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71800-031
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONIC ACID (UNII: S270N0TRQY)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71800-031-03	1 in 1 BOX	02/11/2025
1		7.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 71800-031-06	2 in 1 BOX	02/11/2025
2		15 mL in 1 BOTTLE, PLASTIC; 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	02/11/2025	12/31/2025

Labeler - Innovida Pharmaeutique Corporation (080892908)

Revised: 12/2025

Document Id: 46e0eafa-6970-a863-e063-6294a90a1118

34390-5

Set id: a6f10528-0b4f-4fb3-9904-9c019d078d95

Version: 3

Effective Time: 20251226