PUBLIX MOISTURIZING RELIEF EYE DROPS- carboxymethylcellulose sodium liquid

Publix Moisturizing Relief Eye Drops by

Drug Labeling and Warnings

Publix Moisturizing Relief Eye Drops by is a Otc medication manufactured, distributed, or labeled by Publix Super Markets, Inc., KC Pharmaceuticals, Inc., Unimed. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

Lubricant

Uses

• for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun
• may be used as a protectant against further irritation

Warnings

For external use only

Do not use this product if

• solution changes color or becomes cloudy

When using this product

• do not reuse
• once opened, discard
• to avoid contamination, do not touch tip of container to any surface
• do not touch unit-dose tio to eye

Stop use and ask a doctor if

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye continues
• redness or irritation of the eye worsens or persists for more than 72 hours

Keep out of the reach of children.

If accidentally swallowed, get medical help or contact a Poisin Control Center (1-800-222-1222) immediately.

Directions

• to open, twist and pull tab to remove
• instill 1 or 2 drops in the affected eye(s) as needed and discard container
• if used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor's instructions

Other information

• store at 59°-77°F (15°-25°C)
• use only if single-use container is intact
• use before expiration date marked on container
• RETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive ingredients

calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.

**May contain these ingredients to adjust pH.

Publix Moisturizing Relief Eye Drops 30ct

INGREDIENTS AND APPEARANCE

PUBLIX MOISTURIZING RELIEF EYE DROPS 
carboxymethylcellulose sodium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56062-789
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	0.5 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56062-789-01	30 in 1 BOX	01/01/2020
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 final	part349	01/01/2020

Labeler - Publix Super Markets, Inc. (006922009)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
KC Pharmaceuticals, Inc.		174450460	pack(56062-789) , label(56062-789)

Establishment
Name	Address	ID/FEI	Business Operations
Unimed		689852052	manufacture(56062-789)