Home NDC 79662-002 Rain Renewal Eye Drops
Product NDC 79662-002
11-digit product format 796620002
Labeler code 79662
Product ID 79662-002_4c627fee-62be-a0f0-e063-6294a90a4252
Type HUMAN OTC DRUG
Nonproprietary name carboxymethylcellulose sodium
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Rain Eye Drops, LLC
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-02-15
Substance CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
Active strength .5 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 21 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 79662-002-70 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 79662-002-70 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 79662-002-70 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 79662-002-70 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 79662-002-70 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 79662-002-70 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 79662-002-70 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 79662-002-70 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 79662-002-70 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 79662-002-70 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 79662-002-70 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 79662-002-70 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Rain Renewal Eye Drops
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM .5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K679OBS311 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1188426 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table 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 79662-002-30 Rain Renewal Eye Drops 30 in 1 BOX SOLUTION/ DROPS 30 8 79662-002-30 Rain Renewal Eye Drops 0.4 mL in 1 VIAL, DISPENSING SOLUTION/ DROPS 0.4 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79662-002 RAIN RENEWAL EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [RAIN EYE DROPS, LLC] 9 Current NDC, Legacy NDC, 2 package rows 20231118_af9ef210-7e71-39bd-e053-2995a90a07c9.zip 79662-002 RAIN RENEWAL EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [RAIN EYE DROPS, LLC] 7 Current NDC, Legacy NDC, 2 package rows 20241004_bb451b22-c4f6-291d-e053-2a95a90a7801.zip
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.
Matched openFDA labels page 6 of 25 · 494 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 79662-002-30 79662000230 30 VIAL, DISPENSING in 1 BOX (79662-002-30) > .4 mL in 1 VIAL, DISPENSING 2021-02-15 0000-00-00 No No Current 79662-002-70 79662000270 70 VIAL, DISPENSING in 1 BOX (79662-002-70) > .4 mL in 1 VIAL, DISPENSING 2020-09-18 0000-00-00 No No Current