Doctor Hoys Pain Relief Gel

Product NDC: 75638-010
11-digit product format: 756380010
Labeler code: 75638
Product ID: 75638-010_4769df6d-225f-5a0d-e063-6394a90af652
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL, CAMPHOR (SYNTHETIC)
Dosage form: GEL
Route: TOPICAL
Labeler: Dynamic Blending Specialists, Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-03-01
Marketing end: 2028-04-13
Substance: MENTHOL; CAMPHOR (SYNTHETIC)
Active strength: 50; 50 mg/mL; mg/mL
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 · 15 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
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75638-010-03	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75638-010-02	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75638-010-01	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75638-010-00	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75638-010-03	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75638-010-02	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75638-010-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75638-010-00	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75638-010-03	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75638-010-02	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75638-010-01	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75638-010-00	`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: Doctor Hoys Pain Relief Gel

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	50 mg/mL
CAMPHOR (SYNTHETIC)	50 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
797500	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
50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
75638-010-00	Doctor Hoy's Pain Relief Gel
75638-010-01	Doctor Hoy's Pain Relief Gel
75638-010-02	Doctor Hoy's Pain Relief Gel
75638-010-03	Doctor Hoy's Pain Relief Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75638-010-00	Doctor Hoys Pain Relief Gel	89 mL in 1 TUBE	GEL	89	4
75638-010-01	Doctor Hoys Pain Relief Gel	177 mL in 1 TUBE	GEL	177	4
75638-010-02	Doctor Hoys Pain Relief Gel	946 mL in 1 TUBE	GEL	946	4
75638-010-03	Doctor Hoys Pain Relief Gel	1893 mL in 1 TUBE	GEL	1893	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75638-010	DOCTOR HOYS PAIN RELIEF GEL (MENTHOL, CAMPHOR (SYNTHETIC)) GEL [DYNAMIC BLENDING SPECIALISTS, INC.]	3	Current NDC, 4 package rows	20250201_50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8.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 9 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
REINREUDE BACK PAIN THERAPY	CAMPHOR 80MG MENTHOL 24MG BACK PAIN THERAPY	Jiangxi Yudexi Pharmaceutical Co., LTD	4dfc77bb-11dd-e0f0-e063-6294a90a4e9c	2026-07-24	Warnings	Exact identifier application number: M017
DRAVYNOR QUIT SMOKING Patches	NICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHES	Wenzhou Yuyuan Pharmaceutical Co., Ltd.	5768631f-d517-5b43-e063-6294a90a8f46	2026-07-24	Warnings	Exact identifier application number: M017
DERMFREE NUMBING	LIDOCAINE4% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5b47ce-2bf1-42c7-e063-6294a90af09f	2026-07-23	Warnings	Exact identifier application number: M017
DERMFREE WART CORN REMOVER	SALICYLIC ACID 40% WART CORN REMOVER	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5c63b3-44de-8736-e063-6394a90ac21a	2026-07-23	Warnings	Exact identifier application number: M017
DERMFREE Anti-itch	HYDROCORTISONE1% ANTI-ITCH	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5af4c6-555a-e74c-e063-6394a90aa6ce	2026-07-23	Warnings	Exact identifier application number: M017
DERMFREE HEMORRHOID	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5d0e79-d620-0147-e063-6294a90a3103	2026-07-23	Warnings	Exact identifier application number: M017
MAG 5 PT WARMING FORMULA	MENTHOL	RENU LABORATORIES, LLC	a499ac9b-0e8e-e23f-e053-2a95a90abe9a	2026-07-23	Warnings	Exact identifier application number: M017
Icy Hot Performance Cream Pain Relief	MENTHOL 16%, CAMPHOR 11%	Chattem, Inc.	73f7a113-ef11-4932-bf4d-4e62863f7941	2026-07-23	Warnings	Exact identifier application number: M017
Numbing Pain Relief	LIDOCAINE 4%	Walgreen Company	2425badb-e196-e9f8-e063-6294a90a7bf4	2026-07-22	Warnings	Exact identifier application number: M017
Cooling Pain Relief	MENTHOL 4.5%	Walgreen Company	24345ccf-c96f-31b0-e063-6294a90a82b5	2026-07-22	Warnings	Exact identifier application number: M017
Heat Pain Relief	CAPSAICIN 0.1%	Walgreen Company	2434f9cf-74aa-17af-e063-6294a90a56d9	2026-07-22	Warnings	Exact identifier application number: M017
Pain Relief Patch Lidocaine	LIDOCAINE	HyVee	41c26a66-3371-2c2c-e063-6294a90aa38b	2026-07-22	Warnings	Exact identifier application number: M017
CVS Ultra Strength Muscle	MENTHOL, CAMPHOR, METHYL SALICYLATE	CVS Pharmacy	48bef8bc-6e39-a328-e063-6394a90ae450	2026-07-22	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	AKRON PHARMA INC	daad9a1e-98d2-4ce7-9d97-ac5d81905abb	2026-07-22	Warnings	Exact identifier application number: M017
Professional Therapy MuscleCare Pain Relieving	MENTHOL, CAMPHOR	Active and Innovative	573c2d85-9e0b-7955-e063-6394a90aff64	2026-07-22	Warnings	Exact identifier application number: M017
DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEF	BENZALKONIUM CHLORIDE, LIDOCAINE	Enviro Specialty Chemicals Inc	f7abe66c-dc2d-4ef7-9b11-5b87157fd302	2026-07-21	Warnings	Exact identifier application number: M017
Bclsks NUMBING	MENTHOL 1% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	49e26770-ddf6-7515-e063-6394a90a4ab3	2026-07-21	Warnings	Exact identifier application number: M017
Rstrvbr QUIT SMOKING	NICOTINE21MG QUIT SMOKING	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5e9691-727f-6bcd-e063-6294a90aadfc	2026-07-21	Warnings	Exact identifier application number: M017
Rstrvbr QUIT SMOKING	NICOTINE14MG QUIT SMOKING	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5eec19-7f9a-d277-e063-6294a90ace95	2026-07-21	Warnings	Exact identifier application number: M017
Rstrvbr QUIT SMOKING	NICOTINE7MG QUIT SMOKING	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5f124e-2dd7-16b8-e063-6294a90a5cdb	2026-07-21	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
797500	camphor 5 % / menthol 5 % Topical Gel	PSN	50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8	4
797500	camphor 0.05 MG/MG / menthol 0.05 MG/MG Topical Gel	SCD	50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8	4
797500	camphor 5 % / menthol 5 % Topical Gel	SY	50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
75638-010-00	75638001000	89 mL in 1 TUBE (75638-010-00)	89 ml	2023-03-01	2028-04-13	No	No	Historical
75638-010-01	75638001001	177 mL in 1 TUBE (75638-010-01)	177 ml	2023-03-01	2028-01-24	No	No	Historical
75638-010-02	75638001002	946 mL in 1 TUBE (75638-010-02)	946 ml	2023-03-01	2028-01-24	No	No	Historical
75638-010-03	75638001003	1893 mL in 1 TUBE (75638-010-03)	1893 ml	2023-03-01	2028-01-24	No	No	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Doctor Hoy's Pain Relief Gel	Dynamic Blending Specialists, Inc.	2026-01-02	HUMAN OTC DRUG LABEL	4