Home NDC 79662-001 Rain Renewal Eye Drops
Product NDC 79662-001
11-digit product format 796620001
Labeler code 79662
Product ID 79662-001_2a93998c-1861-9207-e063-6294a90ab0e9
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 2020-09-18
Substance CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
Active strength .5 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 79662-001-30 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 79662-001-30 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 79662-001-30 bd6a592717d7…303034d00443…
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 2026-12-31 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 79662-001-30 Rain Renewal Eye Drops 30 in 1 BOX SOLUTION/ DROPS 30 4 79662-001-30 Rain Renewal Eye Drops 0.4 mL in 1 BOTTLE, UNIT-DOSE SOLUTION/ DROPS 0.4 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79662-001 RAIN RENEWAL EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [RAIN EYE DROPS, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20250101_af7a5768-7d1d-3d93-e053-2a95a90a38f6.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 79662-001-30 79662000130 30 BOTTLE, UNIT-DOSE in 1 BOX (79662-001-30) / .4 mL in 1 BOTTLE, UNIT-DOSE 2020-09-18 0000-00-00 No No Current