OHTRUST ARTIFICAL EYEDROP- sodium chloride liquid

OHTrust Artifical Eyedrop by

Drug Labeling and Warnings

OHTrust Artifical Eyedrop by is a Otc medication manufactured, distributed, or labeled by Nanoplus Limited (Cayman) Taiwan Branch. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Sodium chloride 0.9% (W/V)

Purpose

Lubricant (Artificial Tears)

Warnings

For external use only
- Do not use if solution changes color or becomes cloudy
- Do not touch the tip of the container to any surface to avoid contamination

Uses

- 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

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.

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

Directions

- To open, twist cap to remove
- Instill 1 to 2 drops in the affected eye(s) as needed
- Discard any unused portion

Other Information

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

Inactive Ingredients

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

Package Label

INGREDIENTS AND APPEARANCE

OHTRUST ARTIFICAL EYEDROP 
sodium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70970-008
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)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70970-008-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/27/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	02/27/2025

Labeler - Nanoplus Limited (Cayman) Taiwan Branch (656283417)

Establishment
Name	Address	ID/FEI	Business Operations
Nanoplus Limited (Cayman) Taiwan Branch		656283417	manufacture(70970-008)