DIE DA WAN HUA PAIN RELIEVING

Product NDC: 61821-001
Requested package NDC: 61821-001-01
11-digit product format: 618210001
Labeler code: 61821
Product ID: 61821-001_ceb6a328-0c61-4c6d-9152-3ce51abbd92c
Type: HUMAN OTC DRUG
Nonproprietary name: TURPENTINE
Dosage form: OIL
Route: TOPICAL
Labeler: GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARMACEUTICAL CO., LTD
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2003-05-08
Marketing end: 0000-00-00
Substance: TURPENTINE
Active strength: 6 g/100mL
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	61821-001	61821-001-01	I	Inactivated by FDA		2026-08-03

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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61821-001-01	2025-01-30	C162847	48780-1	2cef2736-741a-d83d-e063-dadaa90ab31f	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61821-001-01	DIE DA WAN HUA PAIN RELIEVING	50 mL in 1 BOTTLE, PLASTIC	OIL	50		2
61821-001-01	DIE DA WAN HUA PAIN RELIEVING	1 in 1 BOX	OIL	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61821-001	DIE DA WAN HUA PAIN RELIEVING (TURPENTINE) OIL [GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARMACEUTICAL CO., LTD]	2	Legacy NDC, 2 package rows	20191114_5217e0f7-8537-408f-972d-96fb54c162dc.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
XJ6RUH0O4G	TURPENTINE	9005-90-7	TURPENTINE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
61821-001-01	61821000101	1 BOTTLE, PLASTIC in 1 BOX (61821-001-01) > 50 mL in 1 BOTTLE, PLASTIC	2003-05-08	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARMACEUTICAL CO., LTD	2019-11-13	HUMAN OTC DRUG LABEL	2