ARTIFICIAL EYEDROP- sodium chloride liquid

ARTIFICIAL EYEDROP by

Drug Labeling and Warnings

ARTIFICIAL EYEDROP by is a Otc medication manufactured, distributed, or labeled by Water Beauty Innovation Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium chloride 0.9%

PURPOSE

Lubricant

INDICATIONS & USAGE

Relieves dryness and irritation of the eye
Provides temporary relief from discomfort due to minor eye irritations or exposure to wind or sun
Helps protect against further eye irritation

WARNINGS

For external use only

Do not touch the tip of the container to any surface to avoid contamination

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

DO NOT USE

if solution changes color or becomes cloudy
if you are allergic to any of the ingredients

STOP USE

and ask a doctor if

– you experience eye pain
– changes in vision, continued redness, or irritation of the eye
– condition worsens or persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

DOSAGE & ADMINISTRATION

​ To open, twist cap to remove
Instill 1 to 2 drops in the affected eye(s) as needed
Discard if solution changes color or becomes cloudy

STORAGE AND HANDLING

Store at 15–30°C (59–86°F)
Do not use if tamper-evident seal is broken or missing

INACTIVE INGREDIENT

Purified water, sodium borate, potassium chloride, calcium chloride, magnesium chloride

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARTIFICIAL EYEDROP 
sodium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87406-003
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	9 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BORATE (UNII: 91MBZ8H3QO)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
WATER (UNII: 059QF0KO0R)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87406-003-01	15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	02/23/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	02/23/2026

Labeler - Water Beauty Innovation Co. Ltd. (657760151)

Registrant - Water Beauty Innovation Co. Ltd. (657760151)

Establishment
Name	Address	ID/FEI	Business Operations
Water Beauty Innovation Co. Ltd.		657760151	manufacture(87406-003)