Lubricant Drops by VELOCITY PHARMA Lubricant Eye Drops

Lubricant Drops by

Drug Labeling and Warnings

Lubricant Drops by is a Otc medication manufactured, distributed, or labeled by VELOCITY PHARMA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LUBRICANT DROPS- propylene glycol solution/ drops 
VELOCITY PHARMA

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Lubricant Eye Drops

• Active Ingredients: Purpose
• Propylene Glycol 0.6%: 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
• for use as a protectant against further irritation or to relieve dryness of the eye
• for use as a lubricant to prevent further irritation or to relieve 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 tip of container to any surface to avoid contamination
• replace cap after each use

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

• eye pain
• changes 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 a Poison Control Center right away.

Directions

• shake well before using
• put 1 or 2 drops in the affected eye(s) as needed
• see side of carton for directions for use
  

Other Information

• store at room temperature

Inactive Ingredients

benzalkonium chloride solution, boric acid, calcium chloride, magnesium chloride, potassium chloride, castor oil, disodium edetate, polyoxyl 40 hydrogenated castor oil, sodium borate, sodium hyaluronate, purified water. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

LUBRICANT DROPS 
propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76168-502
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.06 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BORIC ACID (UNII: R57ZHV85D4)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
CASTOR OIL (UNII: D5340Y2I9G)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM BORATE (UNII: 91MBZ8H3QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76168-502-30	3 in 1 CARTON	11/11/2021	10/25/2023
1		10 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	11/11/2021	10/25/2023

Labeler - VELOCITY PHARMA (962198409)

Revised: 1/2024

Document Id: 0fa85baf-513e-565a-e063-6394a90a326f

34390-5

Set id: 0941224e-fbed-ac3e-e063-6394a90a70bf

Version: 3

Effective Time: 20240123