BASE LABORATORIES CORNEAL FLOW HYPERTONICITY OPHTHALMIC EYE- sodium chloride ointment

Base Laboratories Corneal Flow Hypertonicity Ophthalmic Eye by

Drug Labeling and Warnings

Base Laboratories Corneal Flow Hypertonicity Ophthalmic Eye by is a Otc medication manufactured, distributed, or labeled by Joonem LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• Pull down the lower lid of the affected eye
• Apply a small amount (1/4 inch) of ointment to the inside of eyelid
• Apply every 3 to 4 hours or as directed by a doctor

Other information

• Store at 15-25C (59-77F)
• Keep tightly closed
• Do not Freeze
• Do not use if difficult to dispense or visible particles are seen in the product
• Side effects associated with this product may be reported to the email address below

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:

INGREDIENTS AND APPEARANCE

BASE LABORATORIES CORNEAL FLOW HYPERTONICITY OPHTHALMIC EYE 
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80327-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80327-011-00	3 in 1 CARTON	01/01/2023
1		5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	01/01/2023

Labeler - Joonem LLC (117633878)