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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	79662-002		I	Inactivated by FDA	2026-10-15
excluded package	package	79662-002	79662-002-70	D	Discontinued by firm	2026-10-15
excluded package	package	79662-002	79662-002-30	D	Discontinued by firm	2026-10-15

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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
bb451b22-c4f6-291d-e053-2a95a90a7801	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9e37788c-b1bf-42ae-aac9-b60601606144	Product name	8	20260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
1527ac37-808d-43be-a63e-74e1258dbe46	Product name	9	20250219
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5	Product name	8	20230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
0ec3537a-6c9b-432a-896c-b9ea8723049a	Product name	9	20200701
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
7916de40-e296-41f0-b811-6d0df1a33e2c	Product name	9	20180627
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
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 table
Package NDC	Product	Description	Form	Quantity	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 14 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
carboxymethylcellulose sodium	CARBOXYMETHYLCELLULOSE SODIUM	AvPAK	b479d2ae-4b59-916a-e053-2995a90af8ec	2025-11-11	Warnings	Exact identifier application number: M018
Sodium Chloride	SODIUM CHLORIDE	Rising Pharma Holdings, Inc.	42870188-b1d7-4934-a6c0-310530497dac	2025-11-07	Warnings	Exact identifier application number: M018
Systane Complete PF	PROPYLENE GLYCOL EMULSION	Alcon Laboratories, Inc.	798ffdde-1dba-4a3f-a0b6-937f9e958cca	2025-11-03	Warnings	Exact identifier application number: M018
LACRIFRESH HYDRAPF	GLYCERIN, POVIDONE	AVIZOR, S.A.	41bbd23e-0ec8-eb18-e063-6294a90a46d1	2025-10-27	Warnings	Exact identifier application number: M018
LACRIFRESH HYDRAMAXPF	GLYCERIN, POVIDONE	AVIZOR, S.A.	41be1604-89b4-7ec3-e063-6294a90a3331	2025-10-27	Warnings	Exact identifier application number: M018
Up and Up Dry Eye Relief Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Target Corporation	3b1834e6-75cf-5380-e063-6294a90ad1d5	2025-10-25	Warnings	Exact identifier application number: M018
Up and Up Dry Eye Relief Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Hanlim	420274c6-7bf0-0920-e063-6294a90a30be	2025-10-25	Warnings	Exact identifier application number: M018
Stye	POLYVINYL ALCOHOL AND POVIDONE	Medtech Products Inc.	60c11d3d-df20-4d1c-b425-49a84fecea30	2025-10-23	Warnings	Exact identifier application number: M018
TheraTears Lubricant	CARBOXYMETHYLCELLULOSE SODIUM	MEDTECH PRODUCTS INC	797b0394-2f0f-4733-8d20-ec5bdf3e085d	2025-10-23	Warnings	Exact identifier application number: M018
Advanced Eye Relief Dry Eye Rejuvenation	GLYCERIN PROPYLENE GLYCOL	Bausch & Lomb Incorporated	027969ee-64e4-4b08-bab7-c4cc8ed22f5f	2025-10-23	Warnings	Exact identifier application number: M018
TheraTears Lubricant	CARBOXYMETHYLCELLULOSE SODIUM	MEDTECH PRODUCTS INC	661d8764-8ae6-4229-9485-867553ee8e16	2025-10-23	Warnings	Exact identifier application number: M018
Refresh Relieva Preservative Free	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	3481f9b3-5a90-40d3-80f8-81f51cc864be	2025-10-22	Warnings	Exact identifier application number: M018
Sodium Chloride Normal Salt	SODIUM CHLORIDE	Method Pharmaceuticals	ce84727a-3677-4bf0-e053-2995a90a3ec8	2025-10-21	Warnings	Exact identifier application number: M018
iVIZIA Dry Eye	POVIDONE	Thea Pharma Inc.	1ef73cb1-da48-a713-e063-6294a90afa9d	2025-10-20	Warnings	Exact identifier application number: M018
Walgreens Ultra Lubricant	POLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOL	Walgreens	21dfe061-4533-2061-e063-6394a90a6e73	2025-10-17	Warnings	Exact identifier application number: M018
Walgreens	SODIUM CHLORIDE	Walgreen Company	21dfc2cf-65ae-c3fb-e063-6294a90a0a94	2025-10-17		Exact identifier application number: M018
Xpect Industrial Eye Relief	GLYCERIN, NAPHAZOLINE HCL	Cintas Corporation	a0167d06-7adb-36f4-e053-2a95a90af9ef	2025-09-30	Warnings	Exact identifier application number: M018
Xpect Eyewash	EYEWASH	Cintas Corporation	1d69365d-662b-4248-8fa9-1629451b549a	2025-09-30	Warnings	Exact identifier application number: M018
REFRESH OPTIVE Drops	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	80275190-d717-40ea-905b-5c8fbe986eac	2025-09-15	Warnings	Exact identifier application number: M018
Refresh Relieva PF Xtra	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	b51b8a75-8faa-430f-8f7e-ee58d3d13f2e	2025-09-15	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
K679OBS311	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM	9004-32-4	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1188426	carboxymethylcellulose sodium 0.5 % Ophthalmic Solution	PSN	af9ef210-7e71-39bd-e053-2995a90a07c9	9
1188426	carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution	SCD	af9ef210-7e71-39bd-e053-2995a90a07c9	9
1188426	carboxymethylcellulose sodium 0.5 % Ophthalmic Solution	SY	af9ef210-7e71-39bd-e053-2995a90a07c9	9
1188426	carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution	SY	af9ef210-7e71-39bd-e053-2995a90a07c9	9
1188426	carboxymethylcellulose sodium 0.5 % Ophthalmic Solution	PSN	bb451b22-c4f6-291d-e053-2a95a90a7801	8
1188426	carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution	SCD	bb451b22-c4f6-291d-e053-2a95a90a7801	8
1188426	carboxymethylcellulose sodium 0.5 % Ophthalmic Solution	SY	bb451b22-c4f6-291d-e053-2a95a90a7801	8
1188426	carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution	SY	bb451b22-c4f6-291d-e053-2a95a90a7801	8

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Rain Renewal Eye Drops - 30 ct	Rain Eye Drops, LLC	2026-03-06	HUMAN OTC DRUG LABEL	8
Rain Eye Drops - 70 ct Pack/Label - US	Rain Eye Drops, LLC	2023-11-17	HUMAN OTC DRUG LABEL	9