Rain Renewal Eye Drops Solution/ Drops
NDC Package 79662-002-70
Package Information
Rain Renewal Eye Drops (carboxymethylcellulose sodium) solution/ dropses is a medication used to relieve dry, irritated eyes. This formulation utilizes a solution/ drops delivery system. Marketed by Rain Eye Drops, Llc, this product is identified by NDC 79662-002 and is authorized under FDA application M018.
Identification & Billing
- RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
- RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
- RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 79662 - Rain Eye Drops, Llc
- 79662-002 - Rain Renewal Eye Drops
- 79662-002-70 - 70 VIAL, DISPENSING in 1 BOX / .4 mL in 1 VIAL, DISPENSING
- 79662-002 - Rain Renewal Eye Drops
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (79662-002). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 79662-002-70 identifies a specific commercial package of 70 vial, dispensing in 1 box / .4 ml in 1 vial, dispensing of Rain Renewal Eye Drops, a human over the counter drug labeled by Rain Eye Drops, Llc. This solution/ drops is formulated for ophthalmic use and contains carboxymethylcellulose sodium, unspecified form as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Rain Eye Drops, Llc on February 15, 2021. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
This medication is used to relieve dry, irritated eyes. Common causes for dry eyes include wind, sun, heating/air conditioning, computer use/reading, and certain medications. This product may contain 1 or more of the following ingredients: carboxymethylcellulose, dextran, glycerin, hypromellose, polyethylene glycol 400 (PEG 400), polysorbate, polyvinyl alcohol, povidone, or propylene glycol, among others. Eye lubricants keep the eye moist, help to protect the eye from injury and infection, and decrease symptoms of dry eyes such as burning, itching, and feeling as if something is in the eye.
How is this Rain Eye Drops, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 79662000270. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
