Rain Renewal Eye Drops
- Manufacturer
- Rain Eye Drops, LLC
- Effective date
- 2023-11-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 9
- Source
- full-release
- Hydrated at
- 2026-06-01 00:02:25
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Carboxymethylcellulose sodium 0.5%
OTC - PURPOSE SECTION
Carboxymethylcellulose sodium.............Lubricant
INDICATIONS & USAGE SECTION
- 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 SECTION
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.
OTC - STOP USE SECTION
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
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
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 SECTION
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 SECTION
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
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | PSN | 9 |
| 1188426 | carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution | SCD | 9 |
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | SY | 9 |
| 1188426 | carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution | SY | 9 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79662-002-70 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9d58-d83d-e063-dadaa90ab31f | Rain Eye Drops - 70 ct Pack/Label - US |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79662-002-70 | Rain Renewal Eye Drops | 0.4 mL in 1 VIAL, DISPENSING | SOLUTION/ DROPS | 0.4 | 9 | |
| 79662-002-70 | Rain Renewal Eye Drops | 70 in 1 BOX | SOLUTION/ DROPS | 70 | 9 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Rain Renewal Eye Drops
- carboxymethylcellulose sodium
- CALCIUM CHLORIDE
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
- CARBOXYMETHYLCELLULOSE
- MAGNESIUM CHLORIDE
- WATER
- POTASSIUM CHLORIDE
- SODIUM LACTATE
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79662-002 | 79662-002-70 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM | K679OBS311 | ACTIB |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| WATER | 059QF0KO0R | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| SODIUM LACTATE | TU7HW0W0QT | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Rain Renewal Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Rain Eye Drops, LLC | bb451b22-c4f6-291d-e053-2a95a90a7801 | 2026-03-06 | Warnings | 79662-002 |
| 0a5f5aa5-a98a-83d4-e063-6394a90ac015 | af9ef210-7e71-39bd-e053-2995a90a07c9 | 2023-11-17 | Warnings | 0a5f5aa5-a98a-83d4-e063-6394a90ac015 af9ef210-7e71-39bd-e053-2995a90a07c9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
