RAIN RENEWAL EYE DROPS- carboxymethylcellulose sodium solution/ drops

Rain Renewal Eye Drops by

Drug Labeling and Warnings

Rain Renewal Eye Drops by is a Otc medication manufactured, distributed, or labeled by Rain Eye Drops, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Carboxymethylcellulose sodium 0.5%

PURPOSE

Carboxymethylcellulose sodium.............Lubricant

INDICATIONS & USAGE

• 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

WARNINGS

​ Warnings

For external use only.

• ​Do not use if solution changes color or becomes cloudy.

When using the product

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

STOP USE

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 REACH OF CHILDREN

Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

DOSAGE & ADMINISTRATION

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 SAFETY INFORMATION

Other information

• Store at 15°-25°C (59°-77°F)
• Use only if single-use container is intact
• Use before expiration date marked on container

RETAIN THIS CARTON FOR FUTURE REFERENCE

INACTIVE INGREDIENT

calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate. **May contain these ingredients to adjust pH.

70 ct

INGREDIENTS AND APPEARANCE

RAIN RENEWAL EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79662-002
Route of Administration	OPHTHALMIC

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79662-002-70	70 in 1 BOX	09/18/2020	11/30/2023
1		0.4 mL in 1 VIAL, DISPENSING; 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	09/18/2020

Labeler - Rain Eye Drops, LLC (117579363)