CVS Health Lubricant Eye Drops

CVS Health Lubricant Drops by

Drug Labeling and Warnings

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

Drug Details [pdf]

CVS HEALTH LUBRICANT DROPS- propylene glycol solution/ drops 
VELOCITY PHARMA

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CVS Health Lubricant Eye Drops

Active IngredientsPurpose
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 if you 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

1020

CVS HEALTH LUBRICANT DROPS 
propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76168-714
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.06 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CASTOR OIL (UNII: D5340Y2I9G)  
BORIC ACID (UNII: R57ZHV85D4)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76168-714-101 in 1 CARTON11/11/202110/25/2023
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC: 76168-714-202 in 1 CARTON11/11/202110/25/2023
210 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01811/11/202110/25/2023
Labeler - VELOCITY PHARMA (962198409)

Revised: 1/2024
 

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