BASE LABORATORIES CORNEAL FLOW HYPERTONICITY OPHTHALMIC EYE- sodium chloride ointment 
Joonem LLC

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Base Laboratories Corneal Flow Hypertonicity Ophthalmic Eye Ointment

Drug Facts

Active ingredient

Sodium chloride 3%

Purpose

Hypertonicity agent

Uses:

Temporary relief of corneal edema

Warnings:

For external use only

Do not use

Except under the advice and supervision of a doctor

When using this product

  • It may cause temporary burning and irritation 
  • Replace cap after use
  • To avoid contamination, do not touch top of container to any surface

Stop use and ask a doctor if 

  • Condition worsens or persists for more than 72 hours
  • You experience eye pain, changes in vision, continued redness or irritation of the eye

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Water, Glycerin, Propylene Glycol, Squalane, Sodium Hyaluronate, Dimethicone, Tocopheryl Acetate, Carnosine, Butylene Glycol, Phenoxyethanol, Chlorphenesin, Ubiquinone

Questions or comments?

cs@baselaboratories.com

Package Labeling:

Label0

BASE LABORATORIES CORNEAL FLOW HYPERTONICITY OPHTHALMIC EYE 
sodium chloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80327-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE30 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SQUALANE (UNII: GW89575KF9)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARNOSINE (UNII: 8HO6PVN24W)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
UBIDECARENONE (UNII: EJ27X76M46)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80327-011-003 in 1 CARTON01/01/2023
15 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01801/01/2023
Labeler - Joonem LLC (117633878)

Revised: 2/2024
Document Id: 11e542db-c3a3-aa93-e063-6294a90a445e
Set id: d44e8198-8ba1-46ee-be88-0228368b7640
Version: 3
Effective Time: 20240221
 
Joonem LLC