Label: RAIN RENEWAL EYE DROPS- carboxymethylcellulose sodium solution/ drops
- NDC Code(s): 79662-001-30
- Packager: Rain Eye Drops, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated February 22, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
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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.
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
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Rain Renewal Eye Drops Dry Eye Relief 30ct
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INGREDIENTS AND APPEARANCE
RAIN RENEWAL EYE DROPS
carboxymethylcellulose sodium solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79662-001 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 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:79662-001-30 30 in 1 BOX 09/18/2020 1 0.4 mL in 1 BOTTLE, UNIT-DOSE; 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 09/18/2020 Labeler - Rain Eye Drops, LLC (117579363)