EYES ALIVE LUBRICATING- carboxymethylcellulose sodium, unspecified liquid

Eyes Alive by

Drug Labeling and Warnings

Eyes Alive by is a Otc medication manufactured, distributed, or labeled by RIVIERA PHARMA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

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

Warnings

For external use only

Do not use is solution changes color or becomes cloudy.

When using this product

• to avoid contamination, do not touch tip of container to any surface. Do not reuse. Once open, discard.
• do not touch unit dose tip to eye

Stop use and ask a doctor before use if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the 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

• TWIST AND REMOVE TAB
• Place 1 or 2 drops in the affected eye(s) as needed for relief and discard container.
• If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctors instructions.

Other information

• Use only if single use container is intact.
• Use before expiration date marked on container.
• Store at 59°-86°F (15°-30°C)
• RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Calcium chloride, hydrochloric acid1, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide1, and sodium lactate.

1 May or may not contain this ingredient to adjust pH.

Questions or comments?

800.477.2884, M-F 8AM-5PM Eastern Time

You can always report serious effects to this number.

PRINCIPAL DISPLAY PANEL - 0.6 mL Container Carton

NDC: 83291-200-32

Eyes
Alive™

Lubricating Eye Drops
Carboxymethylcellulose sodium 0.5%

Preservative Free

IMMEDIATE RELIEF FOR
DRY IRRITATED EYES

32 Sterile Single-Use Containers
0.02 fl oz (0.6 mL) each

MADE IN THE USA

INGREDIENTS AND APPEARANCE

EYES ALIVE   LUBRICATING
carboxymethylcellulose sodium, unspecified liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83291-200
Route of Administration	INTRAOCULAR

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

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
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: 83291-200-02	2 in 1 POUCH	06/01/2023
1		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
2	NDC: 83291-200-04	4 in 1 POUCH	06/01/2023
2		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
3	NDC: 83291-200-32	32 in 1 CARTON	06/01/2023
3		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
4	NDC: 83291-200-52	52 in 1 CARTON	06/01/2023
4		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
5	NDC: 83291-200-72	72 in 1 CARTON	06/01/2023
5		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
6	NDC: 83291-200-00	100 in 1 CARTON	06/01/2023
6		0.6 mL in 1 AMPULE; Type 0: Not a Combination Product
7	NDC: 83291-200-08	8 in 1 CARTON	06/01/2023
7		0.6 mL in 1 AMPULE; 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	06/01/2023

Labeler - RIVIERA PHARMA INC (118748772)