PERFECTEARS- carboxymethylcellulose sodium, carboxymethylcellulose liquid

PerfecTears by

Drug Labeling and Warnings

PerfecTears by is a Otc medication manufactured, distributed, or labeled by Cetel Scientific LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Uses

• For temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun
• protectant against further irritation

Warnings

For external use only.

Do not useif solution changes color or becomes cloudy

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
• 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.

KEEP OUT OF REACH OF CHILDREN

Directions

• To open, TWIST AND PULL TAB TO REMOVE.
• Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

Other information

• use before expiration date marked on container.
• store at 59°-86°F (15°-30°C).

Inactive ingredients

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

Product label

INGREDIENTS AND APPEARANCE

PERFECTEARS 
carboxymethylcellulose sodium, carboxymethylcellulose liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84535-001
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
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE	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)
GELATIN (UNII: 2G86QN327L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84535-001-01	0.4 mL in 1 CONTAINER; Type 0: Not a Combination Product	07/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	07/24/2024

Labeler - Cetel Scientific LLC (079453529)