WALGREENS LUBRICANT EYE DROPS PRESERVATIVE FREE- dextran 70, hypromellose liquid 
Walgreen Company

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Walgreens Lubricant Eye Drops Preservative Free (PLD)

Active ingredients

Dextran 70 0.1%

Hypromellose 0.3%

Purposes

Lubricant

Lubricant

Use

Warnings

For external use only

Do not use

  • if this solution changes color or becomes cloudy
  • if you are sensative to any ingredient in this product

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • do not reuse
  • once opened, discard

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

store at 15°-25°C (59°-77°F)

Inactive ingredients

boric acid, disodium edetate hydrate, potassium chloride, purified water, sodium borate, sodium chloride

Questions or comments?

Call 1-888-527-4276

Walgreens Lubricant Eye Drops Preservative Free 35ct

Walgreens Lubricant Eye Drops Preservative Free 35ct

WALGREENS LUBRICANT EYE DROPS PRESERVATIVE FREE 
dextran 70, hypromellose liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0646
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 700.1 g  in 100 mL
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO) HYPROMELLOSE, UNSPECIFIED0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0646-0135 in 1 BOX01/01/2020
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01801/01/2020
Labeler - Walgreen Company (008965063)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460pack(0363-0646) , label(0363-0646)
Establishment
NameAddressID/FEIBusiness Operations
Unimed689852052manufacture(0363-0646)

Revised: 12/2023
Document Id: 0cf96dfd-82db-9204-e063-6394a90a1019
Set id: 9b383e41-e116-1c12-e053-2a95a90ab25f
Version: 2
Effective Time: 20231220
 
Walgreen Company