GOOD SENSE LUBRICATING PLUS LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops 
GoodSense

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GoodSense Lubricating Plus Lubricant Eye Drops (PLD)

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Carboxymethylcellulose sodium ..... 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

Carton

GOOD SENSE LUBRICATING PLUS LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-700
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50804-700-0130 in 1 CARTON07/19/2023
10.4 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01807/19/2023
Labeler - GoodSense (076059836)
Registrant - Unimed Pharmaceuticals, Inc. (689852052)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052pack(50804-700) , label(50804-700) , manufacture(50804-700)

Revised: 12/2023
Document Id: 0d383700-e25a-881f-e063-6294a90a347c
Set id: ffd6428e-3bf5-8742-e053-6394a90a4c8f
Version: 4
Effective Time: 20231223
 
GoodSense