SHANGHAI SHANG SHI ZHI TONG GAO PAIN RELIEVING

Product NDC: 22742-003
Requested package NDC: 22742-003-01
11-digit product format: 227420003
Labeler code: 22742
Product ID: 22742-003_794801f2-3f14-4a96-99e8-b4eef53461c2
Type: HUMAN OTC DRUG
Nonproprietary name: CAMPHOR, MENTHOL, METHYL SALICYLATE
Dosage form: PATCH
Route: TOPICAL
Labeler: SHANGHAI LEI YUN SHANG PHARMACEUTICAL CO LTD
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2009-03-09
Marketing end: 0000-00-00
Substance: CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Active strength: 10 1/1; 1/1; 1/1
NDC exclude flag: No
Listing certified through: 2020-12-31
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	22742-003	22742-003-01	I	Inactivated by FDA		2026-10-20

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 · 19 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…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5dbf91a8-ec29-4ffc-807c-e3bae7fb67b1	Product name	1	20201123
85bed648-23ca-4804-98e6-e36aee999cad	Product name	1	20190717
80de93b4-8a94-428d-beb7-d644353ee70b	Product name	1	20180424
eb4f7d5b-1286-40dc-b8bf-ad87ff51c688	Product name	1	20170522
db8eb201-78c7-4590-8a71-fac0a539bd8c	Product name	1	20170404
141092be-5eb5-452e-9f69-2d350aa70a87	Product name	1	20161208

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
22742-003-01	2021-07-23	C162847	48780-1	c7ccaba7-1d40-fd44-e053-dadaa90aa01b	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
22742-003-01	SHANGHAI SHANG SHI ZHI TONG GAO PAIN RELIEVING	2 in 1 POUCH	PATCH	2		2
22742-003-01	SHANGHAI SHANG SHI ZHI TONG GAO PAIN RELIEVING	3 in 1 BOX	PATCH	3		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
22742-003	SHANGHAI SHANG SHI ZHI TONG GAO PAIN RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) PATCH [SHANGHAI LEI YUN SHANG PHARMACEUTICAL CO LTD]	2	Legacy NDC, 2 package rows	20191114_ef89cd98-630d-4781-927f-861c928e90b8.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1733821	camphor 10 % / menthol 10.28 % / methyl salicylate 15.43 % Medicated Patch	PSN	ef89cd98-630d-4781-927f-861c928e90b8	2
1733821	camphor 0.1 MG/MG / menthol 0.103 MG/MG / methyl salicylate 0.154 MG/MG Medicated Patch	SCD	ef89cd98-630d-4781-927f-861c928e90b8	2
1733821	camphor 10 % / menthol 10.28 % / methyl salicylate 15.43 % Medicated Patch	SY	ef89cd98-630d-4781-927f-861c928e90b8	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
22742-003-01	22742000301	3 POUCH in 1 BOX (22742-003-01) > 2 PATCH in 1 POUCH	3 pouch	2009-03-09	0000-00-00	No	No	Current