CVS HYDRATION EYE DROPS- polyetylene glycol 400, propylene glycol solution/ drops 
CVS

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CVS Hydration Eye Drops 10 mL (PLD)

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

Purposes

Lubricant

Lubricant

Use

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 experience any of the following:

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

Keep out of reach of childeren.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

put 1 or 2 drops in the affected eye(s) as needed

Other information

Store at temperature, not exceeding 59°F (15°C)

Inactive ingredients

boric acid, hypromellose, potassium chloride, purified water, sodium chloride, sodium hyaluronate, sodium hydroxide

CVS Hydration Eye Drops

CVS Hydration Eye Drops

CVS HYDRATION EYE DROPS 
polyetylene glycol 400, propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-615
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 g  in 100 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
BORIC ACID (UNII: R57ZHV85D4)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51316-615-101 in 1 BOX01/19/2023
110 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 DrugM01801/19/2023
Labeler - CVS (062312574)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Unimed688016567manufacture(51316-615) , pack(51316-615) , label(51316-615)

Revised: 12/2023
Document Id: 0d29b49a-71d5-b6b9-e063-6294a90a9247
Set id: ecab8fa3-6575-0dde-e053-2a95a90abd61
Version: 3
Effective Time: 20231223
 
CVS