Royal King Pain Relief Patch

Product NDC: 69412-001
Requested package NDC: 69412-001-03
11-digit product format: 694120001
Labeler code: 69412
Product ID: 69412-001_26a19551-a694-403b-b1fd-0ed18764ba57
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor
Dosage form: PATCH
Route: TOPICAL
Labeler: Tianshui Weishi Tongtai Pharmaceutical Co Ltd
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2016-12-20
Marketing end: 0000-00-00
Substance: CAMPHOR (SYNTHETIC)
Active strength: 0 g/100g
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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	69412-001	69412-001-03	I	Inactivated by FDA		2026-08-03

Observed NDC auxiliary status history#

Observed captured status history: Rows come only from successfully parsed FDA auxiliary ZIP captures. They show the state present in that artifact, not a continuous regulatory timeline. Absence before, after, or between captures is not proof of status, and a known non-data HTTP 403 capture is preserved in backfill provenance but cannot produce a status row.

Historic NDC status page 1 of 1 · 11 matching rows.

Browse every current auxiliary row. · Browse the complete NDC auxiliary source catalog.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Archive	Snapshot	Source SHA-256
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69412-001	69412-001-03	I	Inactivated by FDA	excluded / ndc_excluded.zip	`1332a3947898…`	`d4bfe170f9cd…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69412-001-03	2023-01-30	C162847	48780-1	f386c649-c7d9-0266-e053-dadaa90a7c1a	Tianshui Weishi Tongtai Pharmaceutical Co Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69412-001-03	Royal King Pain Relief Patch	3 in 1 BOX	PATCH	3		32765
69412-001-03	Royal King Pain Relief Patch	7.9 g in 1 PATCH	PATCH	7.9		32765

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69412-001	ROYAL KING PAIN RELIEF PATCH (CAMPHOR) PATCH [TIANSHUI WEISHI TONGTAI PHARMACEUTICAL CO LTD]	32765	Legacy NDC, 2 package rows	20211201_33891e00-3421-42f2-a6d1-383f4aed0e35.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1866042	camphor 0.13 % Medicated Patch	PSN	33891e00-3421-42f2-a6d1-383f4aed0e35	32765
1866042	camphor 0.0013 MG/MG Medicated Patch	SCD	33891e00-3421-42f2-a6d1-383f4aed0e35	32765
1866042	camphor 0.13 % Medicated Patch	SY	33891e00-3421-42f2-a6d1-383f4aed0e35	32765

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69412-001-03	69412000103	3 PATCH in 1 BOX (69412-001-03) > 7.9 g in 1 PATCH	3 patch	2016-12-20	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Tianshui Weishi Tongtai Pharmaceutical Co Ltd	Tianshui Weishi Tongtai Pharmaceutical Co Ltd	2021-11-29	HUMAN OTC DRUG LABEL	32765