S9 SOSEANG-SU

Product NDC: 81612-002
Requested package NDC: 81612-002-01
11-digit product format: 816120002
Labeler code: 81612
Product ID: 81612-002_bc2a44d1-bce2-4a62-e053-2a95a90aac1a
Type: HUMAN OTC DRUG
Nonproprietary name: HYPOCHLOROUS ACID
Dosage form: LIQUID
Route: TOPICAL
Labeler: Sejong Ecosys
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2021-02-25
Marketing end: 0000-00-00
Substance: HYPOCHLOROUS ACID
Active strength: 1 mg/100mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	81612-002	81612-002-01	I	Inactivated by FDA		2026-10-05

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 · 16 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81612-002-01	2022-07-29	C162847	48780-1	e4f33bdf-9ba0-d8a0-e053-dadaa90a6e4e	bc279156-28cf-edc1-e053-2a95a90a3aad
81612-002-02	2022-07-29	C162847	48780-1	e4f33bdf-9ba0-d8a0-e053-dadaa90a6e4e	bc279156-28cf-edc1-e053-2a95a90a3aad
81612-002-03	2022-07-29	C162847	48780-1	e4f33bdf-9ba0-d8a0-e053-dadaa90a6e4e	bc279156-28cf-edc1-e053-2a95a90a3aad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
81612-002-01	S9 SOSEANG-SU	50 mL in 1 BOTTLE, SPRAY	LIQUID	50	2
81612-002-02	S9 SOSEANG-SU	100 mL in 1 BOTTLE, SPRAY	LIQUID	100	2
81612-002-03	S9 SOSEANG-SU	500 mL in 1 BOTTLE, SPRAY	LIQUID	500	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81612-002	S9 SOSEANG-SU (HYPOCHLOROUS ACID) LIQUID [SEJONG ECOSYS]	2	Legacy NDC, 3 package rows	20210226_bc279156-28cf-edc1-e053-2a95a90a3aad.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
712K4CDC10	HYPOCHLOROUS ACID	7790-92-3	HYPOCHLOROUS ACID

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
81612-002-01	81612000201	50 mL in 1 BOTTLE, SPRAY (81612-002-01)	50 ml	2021-02-25	0000-00-00	No	No	Current