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 45 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DZUL - LIDO CREME	LIDOCAINE HCL, MENTHOL	Caball Sales, Inc.	063387e4-a1b1-a467-e063-6294a90a6cbd	2026-01-08	Warnings	Exact identifier application number: M017
TOPICAINE	LIDOCAINE 4%	ESBA LABORATORIES INC.	7f96e980-891e-743d-e053-2a91aa0aea5f	2026-01-08	Warnings	Exact identifier application number: M017
LUBRICAINE	LIDOCAINE 4%	ESBA LABORATORIES INC.	9d7416b1-607d-34e0-e053-2a95a90aa3c3	2026-01-08	Warnings	Exact identifier application number: M017
0.5% LIDOCAINE BURN RELIEF	LIDOCAINE HYDROCHLORIDE	Universal Distribution Center LLC	0a1aeff0-bade-457b-a0ac-099d646c0b2e	2026-01-08	Warnings	Exact identifier application number: M017
4% MENTHOL COLD THERAPY	MENTHOL	Universal Distribution Center LLC	66892993-a755-4584-b2a8-2e8d7ac70593	2026-01-08	Warnings	Exact identifier application number: M017
Private Label Antifungal Barrier Cream	2% MICONAZOLE NITRATE CREAM	Swiss-American CDMO, LLC	e74bddea-c1ac-4e4e-84bd-5a9defb85b2d	2026-01-08	Warnings	Exact identifier application number: M017
2.0% LIDOCAINE BURN	LIDOCAINE HYDROCHLORIDE	Universal Distribution Center LLC	e1911279-85f7-4053-b6da-8f4e991347a2	2026-01-08	Warnings	Exact identifier application number: M017
POMG PAIN RELIEF ROLLER	LIDOCAINE HYDROCHLORIDE, MENTHOL	POMG LLC	1fa980fb-fc0e-fdd0-e063-6394a90adc13	2026-01-07	Warnings	Exact identifier application number: M017
Artridon Glucosamine	MENTHOL, METHYL SALICYLATE	Pharmadel LLC	73572156-4cce-0669-e053-2991aa0aaecc	2026-01-07	Warnings	Exact identifier application number: M017
HealthWise Cooling Pain Relief	MENTHOL	Veridian Healthcare	6e2ad0ab-e3a8-4e3a-8f1d-2cd6351185bd	2026-01-07	Warnings	Exact identifier application number: M017
Hydrocortisone 1% Anti-Itch Cream	HYDROCORTISONE	DLC Laboratories, Inc.	16eeec2c-065d-4da0-e063-6294a90a3873	2026-01-07	Warnings	Exact identifier application number: M017
Maximum Strength Hydrocortisone	HYDROCORTISONE	DLC Laboratories, Inc	caf50f12-f35c-4e9e-8ef7-3b0c84e225ee	2026-01-07	Warnings	Exact identifier application number: M017
EARTHS CARE MUSCLE AND JOINT RUB	CAMPHOR	DLC Laboratories, Inc.	71e33e06-4dc3-4ead-a122-ff89d93a64de	2026-01-07	Warnings	Exact identifier application number: M017
Amour CBD	PAIN RELIEF CREAM	SVD Premium Products	95b45e79-b1e7-17b2-e053-2995a90a8836	2026-01-07	Warnings	Exact identifier application number: M017
Tiger Balm Active Muscle	METHYL SALICYLATE AND MENTHOL, UNSPECIFIED FORM	Haw Par Healthcare Ltd.	845a4ead-f9c0-4009-bcae-b17cd388439b	2026-01-07	Warnings	Exact identifier application number: M017
3X Medicated Toothache and Gum Gel	BENZOCAINE	Rite Aid	996f7989-17ce-5b28-e053-2995a90af8b8	2026-01-06	Warnings	Exact identifier application number: M017
QNTAMAX Muscle and Joint Pain Relieving	CAMPHOR (SYNTHETIC), MENTHOL	Qntamax LLC	6622b94c-824e-4e84-a8d8-b60bb0b866e2	2026-01-06	Warnings	Exact identifier application number: M017
Winco Muscle and Joint Pain Relief Gel 2oz	WINCO BENGAY VANISHING SCENT MUSCLE AND JOINT PAIN RELIEF	WINCO FOODS, LLC	47bedf4e-4036-cf43-e063-6394a90a91d6	2026-01-06	Warnings	Exact identifier application number: M017
Pain Relief Hot Patch	MENTHOL AND CAPSAICIN	Universal Distribution Center LLC	110bcb16-ef0b-4bc8-8877-173a0494e1ad	2026-01-06	Warnings	Exact identifier application number: M017
WOFANLI Quit Smoking Nicotine Patches	NICOTINE PATCHES	Shenzhen Paxi Trading Co., Ltd.	4582b4e9-0c24-069d-e063-6394a90a6f4b	2026-01-05	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