FOCUS TEARS PF- carboxymethylcellulose sodium solution/ drops

Focus Tears PF by

Drug Labeling and Warnings

Focus Tears PF by is a Otc medication manufactured, distributed, or labeled by Covalent Medical, Unither Manufacturing LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Carboxymethylcellulose sodium (0.5%)

Purpose

Eye Lubricant

Warnings

For use in the eyes only.

When using this product

■ do not touch tip of container to any surface to avoid contamination.
■ do not reuse; once opened discard.

Stop use and ask a doctor if

■ you experience eye pain, changes in vision, continued redness or irritation of the eye.
■ tile 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

■ Instill 1 or 2 drops into affected eye(s) as needed and discard container.

Other information

■ Use only if tamper seal on top and bottom flaps are intact.
■ Store between 15°-30°C (59°-86°F).
■ Keep carton for complete product information.

Inactive ingredients

Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

Principal Display Panel

INGREDIENTS AND APPEARANCE

FOCUS TEARS PF 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82724-009
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LACTATE (UNII: TU7HW0W0QT)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82724-009-20	30 in 1 BOX	09/01/2025
1		0.4 mL in 1 VIAL, SINGLE-USE; 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	09/01/2025

Labeler - Covalent Medical (112467517)

Establishment
Name	Address	ID/FEI	Business Operations
Unither Manufacturing LLC		079176615	manufacture(82724-009)