GUTONG TIEGAO PAIN RELIEVING

Product NDC: 68007-301
11-digit product format: 680070301
Labeler code: 68007
Product ID: 68007-301_3fb9de14-62ec-2f82-e063-6294a90a247e
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor and Menthol
Dosage form: PATCH
Route: TOPICAL
Labeler: GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-06-26
Marketing end: 2028-10-31
Substance: CAMPHOR (SYNTHETIC); MENTHOL
Active strength: 248; 100 mg/1; mg/1
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 · 16 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
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	68007-301-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	68007-301-01	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	68007-301-01	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	68007-301-01	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	68007-301-01	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	68007-301-01	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	68007-301-01	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	68007-301-01	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: GUTONG TIEGAO PAIN RELIEVING

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	248 mg/1
MENTHOL	100 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup
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
1788940	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
3adfac16-ea7b-47df-89f5-91bbd09c4fe1	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68007-301-01	2025-09-27	C162847	48780-1	2cef2736-81a5-d83d-e063-dadaa90ab31f	DRUG FACTS
68007-301-01	2025-01-30	C162847	48780-1	2cef2736-81a5-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68007-301-01	GUTONG TIEGAO PAIN RELIEVING	2 in 1 POUCH	PATCH	2		4
68007-301-01	GUTONG TIEGAO PAIN RELIEVING	3 in 1 BOX	PATCH	3		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68007-301	GUTONG TIEGAO PAIN RELIEVING (CAMPHOR AND MENTHOL) PATCH [GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD]	2	Current NDC, Legacy NDC, 2 package rows	20180712_3adfac16-ea7b-47df-89f5-91bbd09c4fe1.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 90 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Re-Lieved Lidocaine Patch	LIDOCAINE PATCH 4%	Transfer Technology	37ef02d4-2ff5-cb23-e063-6294a90a68af	2025-06-19	Warnings	Exact identifier application number: M017
Post-Treatment Repair Cream	HYDROCORTISONE	Vi Medical Products Inc.	ab8885a9-0778-28ff-e053-2995a90a2e12	2025-06-19	Warnings	Exact identifier application number: M017
MyDerm	LIDOCAINE	Inspec Solutions LLC.	82d075d1-c92e-2097-e053-2991aa0ab131	2025-06-18	Warnings	Exact identifier application number: M017
Walgreens Extra Small Lidocaine	LIDOCAINE	Walgreen Co.	dc838e47-d234-4ba5-9449-f645e99be923	2025-06-18	Warnings	Exact identifier application number: M017
CLn Body Moisturizer	COLLOIDAL OAT MOISTURIZER	TopMD Skin Care, Inc.	2de3d68d-a540-d456-e063-6394a90a4b57	2025-06-18	Warnings	Exact identifier application number: M017
Aloe UP SPF 30 Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35967b33-bdfb-ee3c-e063-6294a90a75f6	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35b9dcfa-05f3-3d7b-e063-6394a90a18f1	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Mineral	ZINC OXIDE	Aloe International, LLC	35bc3621-f4e4-42d3-e063-6394a90a7aad	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Kids Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35cd16b0-bd81-8f68-e063-6294a90a3d8c	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Kids Mineral	ZINC OXIDE	Aloe International, LLC	35cd5542-947d-a042-e063-6394a90a13f8	2025-06-18	Warnings	Exact identifier application number: M017
Relieve Your Pain	MENTHOL	Proximity Capital Partners LLC dba Asutra	c12369dd-8305-edaf-e053-2995a90a0d3d	2025-06-18	Warnings	Exact identifier application number: M017
Melt Pain Away	CAPSAICIN	Proximity Capital Partners LLC dba Asutra	a95a11d7-a2ae-6654-e053-2a95a90a802c	2025-06-18	Warnings	Exact identifier application number: M017
Recovery Roll-On	MENTHOL, CAMPHOR	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	ebc9630f-6d8b-e4f0-e053-2995a90a0b49	2025-06-18	Warnings	Exact identifier application number: M017
ProCure Hydrocortisone 1%	HYDROCORTISONE	Twin Med LLC	37cdfabc-1fdb-246a-e063-6394a90a008a	2025-06-17	Warnings	Exact identifier application number: M017
ProCure Hydrocortisone 1%	HYDROCORTISONE	Twin Med LLC	37ce6c35-b211-43de-e063-6294a90ab773	2025-06-17	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE CREAM 1%	Sun Pharmaceutical Industries, Inc.	312ddc8d-100e-cfac-e063-6294a90acd09	2025-06-16	Warnings	Exact identifier application number: M017
Curist 5% Lidocaine	LIDOCAINE 5%	Little Pharma, Inc.	f20241a2-c5b1-f124-e053-2995a90a891b	2025-06-16	Warnings	Exact identifier application number: M017
Toast Screamin Menthol	MENTHOL	IDEAZ, LLC	37b48b1a-ef3d-afdc-e063-6294a90a6610	2025-06-16	Warnings	Exact identifier application number: M017
Toast Freezin Cold	MENTHOL, METHYL SALICYLATE	IDEAZ, LLC	37b4d363-0099-8cd3-e063-6394a90a18d6	2025-06-16	Warnings	Exact identifier application number: M017
Earths Care Anti-Itch	CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM	DLC Laboratories, Inc.	ba65f58a-d590-498a-b8e7-a3d78935d880	2025-06-13	Warnings	Exact identifier application number: M017

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
1788940	camphor 3.1 % / menthol 1.25 % Medicated Patch	PSN	3adfac16-ea7b-47df-89f5-91bbd09c4fe1	4
1788940	camphor 0.031 MG/MG / menthol 0.0125 MG/MG Medicated Patch	SCD	3adfac16-ea7b-47df-89f5-91bbd09c4fe1	4
1788940	camphor 3.1 % / menthol 1.25 % Medicated Patch	SY	3adfac16-ea7b-47df-89f5-91bbd09c4fe1	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68007-301-01	68007030101	3 POUCH in 1 BOX (68007-301-01) / 2 PATCH in 1 POUCH	3 pouch	2022-06-26	2028-10-31	No	No	Current