CVS LUBRICANT EYE DROPS ORIGINAL- polyethylene glycol 400, propylene glycol solution 
CVS

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CVS Lubricant Eye Drops Original 30 ct. (PLD)

Active ingredients

Polyethylene glycol 400.....0.4%
Propylene glycol.................0.3%

Purposes

Polyethylene glycol 400....Lubricant
Propylene glycol................Lubricant

Use

Warnings

For external use only

Do not use

  • if this solution changes 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 feel eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse or lasts more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

boric acid, hydrochloric acid**, hypromellose, potassium chloride, purified water, sodium chloride, sodium hydroxide**

**May contain these ingredients to adjust pH.

30 ct carton

CVS LUBRICANT EYE DROPS ORIGINAL 
polyethylene glycol 400, propylene glycol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-746
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.4 g  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
BORIC ACID (UNII: R57ZHV85D4)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-746-0130 in 1 CARTON02/12/2021
10.4 mL in 1 VIAL, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01802/12/2021
Labeler - CVS (062312574)
Registrant - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052manufacture(69842-746) , pack(69842-746) , label(69842-746)

Revised: 12/2023
Document Id: 0d378c3a-a2a7-2c6e-e063-6294a90a3a73
Set id: bb1ad35a-79ea-639f-e053-2995a90a96f3
Version: 4
Effective Time: 20231223
 
CVS