RAIN RENEWAL EYE DROPS- carboxymethylcellulose sodium solution/ drops 
Rain Eye Drops, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Rain Renewal Eye Drops Dry Eye Relief - 30ct (PLD)

Active ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

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

Uses

Warnings

For external use only.

When using the product

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 tip 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 reach of children.

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

Directions

Other information

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.

Questions or comments?

Call 1-800-294-0771 or email: Support@tryrain.com

Rain Renewal Eye Drops Dry Eye Relief 30ct

Rain Renewal

RAIN RENEWAL EYE DROPS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79662-001
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
WATER (UNII: 059QF0KO0R)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79662-001-3030 in 1 BOX09/18/2020
10.4 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/18/2020
Labeler - Rain Eye Drops, LLC (117579363)

Revised: 2/2023
Document Id: f55092be-6bd0-c13d-e053-2a95a90a45cb
Set id: af7a5768-7d1d-3d93-e053-2a95a90a38f6
Version: 2
Effective Time: 20230222
 
Rain Eye Drops, LLC