CVS Lubricating Gel Drops

CVS by

Drug Labeling and Warnings

CVS by is a Otc medication manufactured, distributed, or labeled by Velocity Pharma LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CVS- polyethylene glycol 400 and propylene glycol gel 
Velocity Pharma LLC

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CVS Lubricating Gel Drops

Active IngredientsPurpose
Polyethylene Glycol 400 0.4%           Lubricant
Propylene Glycol 0.3% Lubricant

Uses

  • for the temporary relief of burning and irritation due to dryness of the eye
  • for use as a protectant against 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:

  • you feel 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

Other information

  • store at room temperature

Inactive ingredients

Boric Acid, Calcium Chloride, Disodium edetate, Hypromellose, Magnesium Chloride, Potassium Chloride, Purified Water, Sodium borate, Sodium Chloride, Stabilized oxychloro complex, Zinc chloride may contain hydrochloric acid and/or Sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

1

CVS 
polyethylene glycol 400 and propylene glycol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76168-712
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4004 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76168-712-1010 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/14/202110/25/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01806/14/202110/25/2023
Labeler - Velocity Pharma LLC (962198409)
Registrant - Velocity Pharma LLC (962198409)

Revised: 1/2024
Document Id: 0fa82f0d-035d-52f1-e063-6394a90aba80
Set id: b53a2416-9620-4e28-945a-72eec6a50956
Version: 6
Effective Time: 20240123
 
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