YUN XIANG JING

Product NDC: 59321-033
11-digit product format: 593210033
Labeler code: 59321
Product ID: 59321-033_4dec2f72-e9bc-4fb9-b0c8-ed1ab3d521a5
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: LINIMENT
Route: PERCUTANEOUS; TRANSDERMAL
Labeler: GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2002-10-08
Marketing end: 0000-00-00
Substance: MENTHOL
Active strength: 3 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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	59321-033		D	Discontinued by firm		2026-10-16
excluded package	package	59321-033	59321-033-01	D	Discontinued by firm		2026-10-16

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 · 4 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	59321-033-01	`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	59321-033-01	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
CHINESE CINNAMON	INACTIVE INGREDIENT	WS4CQ062KM	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
ENTADA PHASEOLOIDES WHOLE	INACTIVE INGREDIENT	676S281WTB	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
SPARGANIUM STOLONIFERUM ROOT	INACTIVE INGREDIENT	66ZQ85S65H	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
TINOSPORA CAPILLIPES ROOT	INACTIVE INGREDIENT	U65RN3L8Q5	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59321-033	YUN XIANG JING (MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	3	Legacy NDC	20241127_36a9d533-1d00-4640-a764-c6d507a0b31c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59321-033-01	59321003301	30 mL in 1 BOTTLE (59321-033-01)	30 ml	2002-10-08	0000-00-00	No	No	Current