Sodium Chloride

Product NDC: 0363-0193
11-digit product format: 003630193
Labeler code: 0363
Product ID: 0363-0193_43f4dd02-20e9-ee0b-e063-6294a90ad917
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Chloride
Dosage form: SOLUTION/ DROPS
Route: OPHTHALMIC
Labeler: Walgreen Company
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-04-01
Substance: SODIUM CHLORIDE
Active strength: 50 mg/mL
Pharmacologic classes: Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
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 · 22 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0363-0193-13	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0363-0193-13	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0363-0193-13	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0363-0193-13	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0363-0193-13	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0363-0193-13	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0363-0193-13	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0363-0193-13	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0363-0193-13	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0363-0193-13	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0363-0193-13	`367a005e9d99…`	`383a685ebd0f…`

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: Sodium Chloride
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM CHLORIDE	50 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
451W47IQ8X	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
730780	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
d112a344-33cc-41d3-bae6-492631ebdba7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3	Product name	3	20250124
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
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
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
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
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	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
b060cc1a-fe47-856b-0b77-4448b5963de8	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
0363-0193-13	2025-12-20	C162847	48780-1	1e7a6dab-19f1-a2ce-e063-dadaa90aadf7	Walgreens Sodium Chloride Ophthalmic Solution
0363-0193-13	2024-07-30	C162847	48780-1	1e7a6dab-19f1-a2ce-e063-dadaa90aadf7	Walgreens Sodium Chloride Ophthalmic Solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-0193-13	Sodium Chloride	15 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	15		7
0363-0193-13	Sodium Chloride	1 in 1 BOX	SOLUTION/ DROPS	1		7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0363-0193-13	ML - Milliliter	0363-0193	4efcbdfb-3131-47f0-9c61-e285f41878bb	1	2022-06-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0193	SODIUM CHLORIDE SOLUTION/ DROPS [WALGREEN COMPANY]	6	Current NDC, Legacy NDC, 2 package rows	20230506_d112a344-33cc-41d3-bae6-492631ebdba7.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 13 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Equate Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	Walmart	443e214b-2680-79a9-e063-6294a90a68ba	2025-12-20	Warnings	Exact identifier application number: M018
Equate Redness and Dry Eye Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Walmart	44155cf8-6fd9-d16f-e063-6394a90ac731	2025-12-20	Warnings	Exact identifier application number: M018
Original Redness Reliever	TETRAHYDROLIZINE HCL	Walmart	4414f768-0c69-d041-e063-6294a90a5bd9	2025-12-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant	POLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOL	Walgreens	21dfe061-4538-2061-e063-6394a90a6e73	2025-12-19	Warnings	Exact identifier application number: M018
Artificial Tears	GLYCERIN	Geri-Care Pharmaceuticals, Corp	7cc437e3-bad9-59be-e053-2991aa0a1da3	2025-12-19	Warnings	Exact identifier application number: M018
Signature Care Eye Drops Redness and Dry Eye Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Better Living Brands LLC	901f3bbe-e1bb-4e44-879c-711e59813a7f	2025-12-19	Warnings	Exact identifier application number: M018
STYE RELIEF SERUM	CARBOXYMETHYLCELLULOSE SODIUM(CMC)	Guangzhou Shimei Cosmetics Co., Ltd.	45fa7962-b489-4613-e063-6394a90a59b0	2025-12-15	Warnings	Exact identifier application number: M018
Gentle Eyes Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	TRP Company	13f99af6-b7d8-a092-e063-6394a90a5daa	2025-12-15	Warnings	Exact identifier application number: M018
Artificial Tears	GLYCERIN	NuCare Pharmaceuticals,Inc.	97a3d8e2-b2c0-3f5d-e053-2a95a90ac49d	2025-12-15	Warnings	Exact identifier application number: M018
Eyelash Serum	EYELASH SERUM	FlexiGo Inc	4544adf7-bb24-cb10-e063-6294a90aa414	2025-12-06	Warnings	Exact identifier application number: M018
Redness Reliever, Circle K	TETRAHYDROZOLINE HYDROCHLORIDE LIQUID	Lil' Drug Store products, Inc.	44e95d70-f633-1e4e-e063-6294a90a9f21	2025-12-01	Warnings	Exact identifier application number: M018
Splash Pure PF	PROPYLENE GLYCOL	LABORATORIOS SOPHIA, S.A. DE C.V.	40ad7ae5-1f2a-e3b1-e063-6294a90a6f84	2025-11-26	Warnings	Exact identifier application number: M018
Eyewash Station Additive Concentrate	CHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOL	Niagara Pharmaceuticals Inc.	362a6b6d-862d-4322-87a8-5b3a07fbe174	2025-11-24	Warnings	Exact identifier application number: M018
Rain Daily Hydration and Comfort For Dry Eyes	GLYCERIN	Rain Eye Drops, LLC	31d7c204-fb74-fb28-e063-6294a90ab330	2025-11-23	Warnings	Exact identifier application number: M018
Eyewash Additive Concentrate	WATER AND PROPYLENE GLYCOL	Haws Corporation	dd168403-398c-41ff-b1df-d93e4ff39de3	2025-11-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walgreen Company	a39864a3-2407-7b7e-e053-2a95a90ab92f	2025-11-19	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walgreen Company	a39919d5-84db-05df-e053-2995a90ab1d2	2025-11-19	Warnings	Exact identifier application number: M018
Sodium Chloride	SODIUM CHLORIDE	Walgreen Company	d112a344-33cc-41d3-bae6-492631ebdba7	2025-11-19	Warnings	Exact identifier application number: M018 ndc (product): 0363-0193
Eyesaline Eyewash Concentrate	PURIFIED WATER	Honeywell Safety Products USA, Inc.	3765c251-eb14-d60f-e063-6294a90a6a4d	2025-11-12	Warnings	Exact identifier application number: M018
Eyesaline Emergency Eyewash	PURIFIED WATER	Honeywell Safety Products USA, Inc.	37f244fd-c02f-e66a-e063-6394a90aed81	2025-11-12	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
451W47IQ8X	SODIUM CHLORIDE	7647-14-5	SODIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
730780	sodium chloride 5 % Ophthalmic Solution	PSN	d112a344-33cc-41d3-bae6-492631ebdba7	7
730780	sodium chloride 0.854 MEQ/ML Ophthalmic Solution	SCD	d112a344-33cc-41d3-bae6-492631ebdba7	7
730780	NaCl 0.854 MEQ/ML Ophthalmic Solution	SY	d112a344-33cc-41d3-bae6-492631ebdba7	7
730780	NaCl 5 % Ophthalmic Solution	SY	d112a344-33cc-41d3-bae6-492631ebdba7	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0193-13	00363019313	1 BOTTLE, DROPPER in 1 BOX (0363-0193-13) / 15 mL in 1 BOTTLE, DROPPER	2019-04-01	0000-00-00	No	No	Current