CHING WAN HUNG SOOTHING HERBAL BALM

Product NDC: 33217-001
11-digit product format: 332170001
Labeler code: 33217
Product ID: 33217-001_3ab610b2-31c8-f996-e063-6394a90aa7c1
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: OINTMENT
Route: TOPICAL
Labeler: TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-10-25
Marketing end: 2028-10-26
Substance: MENTHOL
Active strength: 1 g/100g
NDC exclude flag: No
Current FDA listing: Yes

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 · 28 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	33217-001-02	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	33217-001-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	33217-001-03	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	33217-001-02	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	33217-001-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	33217-001-03	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	33217-001-02	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	33217-001-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	33217-001-03	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	33217-001-02	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	33217-001-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	33217-001-03	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	33217-001-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	33217-001-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	33217-001-03	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	33217-001-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	33217-001-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	33217-001-03	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	33217-001-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	33217-001-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	33217-001-03	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: CHING WAN HUNG SOOTHING HERBAL BALM

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
418610	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
33217-001-01	2025-07-24	Drug Facts
33217-001-02	2025-07-24	Drug Facts
33217-001-03	2025-07-24	Drug Facts
33217-001-01	2025-01-30	Drug Facts
33217-001-02	2025-01-30	Drug Facts
33217-001-03	2025-01-30	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
33217-001-01	CHING WAN HUNG SOOTHING HERBAL BALM	10 g in 1 TUBE	OINTMENT	10	4
33217-001-02	CHING WAN HUNG SOOTHING HERBAL BALM	30 g in 1 JAR	OINTMENT	30	4
33217-001-03	CHING WAN HUNG SOOTHING HERBAL BALM	3 g in 1 TUBE	OINTMENT	3	4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
ANGELICA SINENSIS ROOT	INACTIVE INGREDIENT	B66F4574UG	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
MYRRH	INACTIVE INGREDIENT	JC71GJ1F3L	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
PISTACIA LENTISCUS RESIN	INACTIVE INGREDIENT	7446H202QW	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
QUINCE	INACTIVE INGREDIENT	12MCS4H09N	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
SAFFLOWER	INACTIVE INGREDIENT	4VBL71TY4Y	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
SANGUISORBA OFFICINALIS TOP	INACTIVE INGREDIENT	09Q902660M	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
SESAME OIL	INACTIVE INGREDIENT	QX10HYY4QV	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1
YELLOW WAX	INACTIVE INGREDIENT	2ZA36H0S2V	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
33217-001	CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.]	2	Current NDC, Legacy NDC, 3 package rows	20181016_ffadc904-8e9d-4cb8-815a-d583bbdb3f0b.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 87 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Good Neighbor Pharmacy Hydrocortisone with Aloe	HYDROCORTISONE	AmerisourceBergen	0c544792-63d9-400c-9888-207c44fdc75e	2025-07-08	Warnings	Exact identifier application number: M017
Good Neighbor Pharmacy Hydrocortisone	HYDROCORTISONE	AmerisourceBergen	58b0b7ba-e547-4e0f-b04d-8e1e6a5d4fcf	2025-07-08	Warnings	Exact identifier application number: M017
Publix Hydro	HYDROCORTISONE	Publix Super Markets Inc	29296b0f-0eed-4bb9-8727-c25c2bcf9fd6	2025-07-08	Warnings	Exact identifier application number: M017
Publix hydro plus	HYDROCORTISONE	Publix Super Markets Inc	a00d82c1-6b09-424a-be78-2603eee3fb9d	2025-07-08	Warnings	Exact identifier application number: M017
Tattoo	TATTOO CREAM	Perfso (HK) Co., Limited	39773cab-12df-4520-e063-6294a90abc5b	2025-07-08	Warnings	Exact identifier application number: M017
Neutrogena Sun Rescue After Sun Medicated Relief	CAMPHOR (SYNTHETIC)	Kenvue Brands LLC	c95c5b64-b90f-1143-e053-2a95a90aa03c	2025-07-07	Warnings	Exact identifier application number: M017
sunmark Hydrocortisone	HYDROCORTISONE	Strategic Sourcing Services LLC	210079e9-3d2f-4489-b468-b96b145034ed	2025-07-07	Warnings	Exact identifier application number: M017
Relief Gel	LIDOCAINE HCL	Good Clean Love, Inc.	e5fa2265-ccb7-750c-e053-2995a90aa51e	2025-07-07	Warnings	Exact identifier application number: M017
Hydrocortisone Plus 12 Moisturizers	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	09ac2749-a60f-4039-8c80-a0d2eaf50c34	2025-07-07	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	2ada9ec2-1c28-4da2-8639-07b3193ffb32	2025-07-03	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	caa2fd64-e262-4d7c-ad8a-69f506feba8c	2025-07-03	Warnings	Exact identifier application number: M017
Stopain Extra Strength	MENTHOL	Troy Manufacturing, Inc.	07e9a235-6d10-4407-8729-beaf936e97ad	2025-07-03	Warnings	Exact identifier application number: M017
Blue Ice Topical Analgesic Gel	ICE GEL	International Wholesale	397cd306-078d-5b7d-e063-6294a90a8bbc	2025-07-03	Warnings	Exact identifier application number: M017
LIDOCAINE	LIDOCAINE, MENTHOL	Vive Health LLC	236ccc6d-21b7-6153-e063-6394a90a4634	2025-07-02	Warnings	Exact identifier application number: M017
AsperFlex MAX	LIDOCAINE 4% WITH MENTHOL 1%	Akron Pharma Inc.	ccf6172b-350a-4b78-b844-f84bf17c491f	2025-07-02	Warnings	Exact identifier application number: M017
METHYL SALICYLATE 25%	METHYL SALICYLATE	Oncora Pharma, LLC	3766e3a9-94a8-4c3e-e063-6394a90aa24a	2025-07-01	Warnings	Exact identifier application number: M017
Diphenhydramine Hydrochloride and Zinc Acetate	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Sun Pharmaceutical Industries, Inc.	c89e3de8-7d71-485c-8fc5-2832d6024f16	2025-07-01	Warnings	Exact identifier application number: M017
Westlake Outdoor Pain and Itch Relieving	LIDOCAINE 4% PAIN AND ITCH RELIEVING	WESTLAKE HB PHARMA	3c563b28-4f4f-9d0c-e063-6294a90adf73	2025-07-01	Warnings	Exact identifier application number: M017
Cortizone 10 Water Resistant	HYDROCORTISONE	Chattem, Inc.	118e55e7-241f-44c4-959e-09bf6221bd77	2025-07-01	Warnings	Exact identifier application number: M017
Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	38c1616e-3b09-0669-e063-6294a90a2c86	2025-06-29	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
418610	menthol 1 % Topical Ointment	PSN	ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	4
418610	menthol 0.01 MG/MG Topical Ointment	SCD	ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	4
418610	menthol 1 % Topical Ointment	SY	ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	4
418610	menthol 1 % Topical Stick	SY	ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
33217-001-01	33217000101	10 g in 1 TUBE (33217-001-01)	10 g	2023-10-25	2028-10-26	No	No	Current
33217-001-02	33217000102	30 g in 1 JAR (33217-001-02)	30 g	2023-10-25	2028-10-26	No	No	Current
33217-001-03	33217000103	3 g in 1 TUBE (33217-001-03)	3 g	2023-10-25	2028-10-26	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.	2025-07-24	HUMAN OTC DRUG LABEL	4