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.

• to avoid contamination do not touch tip of container to any surface
• do not touch unit-dose tip to eye.
• do not reuse
• once opened, discard
• ​do not use if solution changes color or becomes cloudy.
• remove contact lenses before using

Stop Use and ASK Doctor if

• you feel eye pain
• changes in vision occurs
• continued redness or irritations of the eye last
• conditions worsens or last more than 72 hours

STOP USE

Stop use and ask a doctor if

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye lasts
• conditions worsens or lasts 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
• Children under 6 years of age; ask a doctor

OTHER SAFETY INFORMATION

Other information

• Store at 15°-30°C (59°-86°F)
• Protect from light

RETAIN THIS CARTON FOR FUTURE REFERENCE

INACTIVE INGREDIENT

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

Rain Renewal Eye Drops - 30 Ct - Updated package

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79662-002-30	30 in 1 BOX	02/15/2021
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	02/15/2021

Labeler - Rain Eye Drops, LLC (117579363)