GOOD NEIGHBOR PHARMACY LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops 
Amerisource Bergen Drug Corp.

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Good Neighbor Pharmacy Lubricant Eye Drops 30ct (PLD)

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Lubricant

Uses

Warnings

For external use only

Do not use this product if

  • solution changes color or becomes cloudy

When using this product

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

Stop use and ask a doctor if

  • you experience eye pain
  • changes in vision occur
  • redness or irritation of the eye continues
  • redness or irritation of the eye worsens or persists for more than 72 hours

Keep out of the reach of children.

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

Directions

Other information

Inactive ingredients

calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.

**May contain these ingredients to adjust pH.

Questions or comments?

Call 1-888-527-4276

Good Neighbor Pharmacy Lubricant Eye Drops 30ct

Good Neighbor Pharmacy Lubricant Eye Drops 30ct

GOOD NEIGHBOR PHARMACY LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-756
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-756-5630 in 1 BOX06/01/2023
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 DrugM01806/01/2023
Labeler - Amerisource Bergen Drug Corp. (007914906)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460pack(46122-756) , label(46122-756)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052manufacture(46122-756)

Revised: 12/2023
Document Id: 0d3833f2-09ae-7818-e063-6294a90abe9c
Set id: fd2dc23f-6ccc-2644-e053-6294a90a889e
Version: 2
Effective Time: 20231223
 
Amerisource Bergen Drug Corp.