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 11 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
OWELL NATURALS NEUROPATHY MAXIMUM STRENGTH	MENTHOL	OWELL NATURAL 8 LLC	56b8d0cc-2f35-7d38-e063-6294a90ad06d	2026-07-16	Warnings	Exact identifier application number: M017
ANTIPHLAMINE	L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE	Masaem Company	56b93c89-295b-f33a-e063-6294a90a5fe4	2026-07-16	Warnings	Exact identifier application number: M017
Meriwether Skin Pain Relief	MENTHOL, UNSPECIFIED FORM	Meriwether Skin LLC	f6e155be-5879-4176-bb0e-e364f2e5cdf9	2026-07-16	Warnings	Exact identifier application number: M017
Medi-First Muscle Rub Cream	MENTHOL, METHYL SALICYLATE	Unifirst First Aid Corporation	56a6b8b2-7ab0-9854-e063-6294a90ab5ba	2026-07-15	Warnings	Exact identifier application number: M017
Painsil Pain Relief Roll-On	LIDOCAINE HYDROCHLORIDE	Painsil LLC	dee39dff-5749-4ef2-a9ed-182f25e01f67	2026-07-14	Warnings	Exact identifier application number: M017
VARICOSE VEINS MAXIMUM STRENGTH	MENTHOL	OWELL NATURAL & LLC	5692914f-1b14-e3e3-e063-6394a90a94bf	2026-07-14	Warnings	Exact identifier application number: M017
ZyloRelief	LIDOCAINE HYDROCHLORIDE	Highmark Pharma LLC	635f5b98-f74c-495f-a537-686fcba9ccad	2026-07-14	Warnings	Exact identifier application number: M017
ENOKON PAIN RELIEF Spray.	PAIN RELIEF SPRAY.	Henan Enokon Medical Instrument Co., Ltd.	5675ec21-b947-2206-e063-6294a90aa509	2026-07-12	Warnings	Exact identifier application number: M017
Topcare Pain Relief Patch	PAIN RELIEF PATCH MEDICATED 5% MENTHOL	76162	4f00d0b8-d2f4-843b-e063-6294a90a332b	2026-07-12	Warnings	Exact identifier application number: M017
Penetral Roll-on	CAPSAICIN 0.025%	PureTek Corporation	56204c03-8b15-a8b5-e063-6394a90a8189	2026-07-10	Warnings	Exact identifier application number: M017
Intensive Healing Itch Relief	ITCH RELIEF CREAM	NeilMed Pharmaceuticals Inc	563ef1d5-2180-bc45-e063-6294a90a813d	2026-07-10	Warnings	Exact identifier application number: M017
AVON Foot Works Arthritis Achy Foot and Muscle	METHYL SALICYLATE	COSMAX USA, CORPORATION	56440d3f-bc93-cebb-e063-6294a90a5f79	2026-07-10	Warnings	Exact identifier application number: M017
CHEONG KUN PAIN RELIEVING	CAMPHOR	CHEONG KUN PAIN RELIEVER OIL CHINESE MEDICINE FACTORY (MACAU) LIMITED	557d5cb3-2a05-4f45-e063-6394a90a9b12	2026-07-10	Warnings	Exact identifier application number: M017
Biofreeze Professional	MENTHOL	Reckitt Benckiser LLC	485c8208-c93b-5b84-e063-6394a90ab77a	2026-07-10	Warnings	Exact identifier application number: M017
Fit Mist Pain Relief	MENTHOL	Aroma Sensations Inc	f5a98544-8bd7-42dc-a594-5559e3920e29	2026-07-09	Warnings	Exact identifier application number: M017
Nuturna Sciatica	MENTHOL	Micelle Laboratories, Incorporated	ff200864-bedf-4138-bdec-2b23701406dd	2026-07-09	Warnings	Exact identifier application number: M017
Lidocaine cream	DRS LIDOCAINE 5% CREAM	OL PHARMA TECH LLC. (Drs. Pharmacy)	372fe018-1e5a-9ec4-e063-6294a90a1500	2026-07-09	Warnings	Exact identifier application number: M017
Nupharmisto 4% Lidocaine Numbing cream	LIDOCAINE 4%	EveryMarket Inc	5615e49d-e03b-f915-e063-6294a90a1786	2026-07-08	Warnings	Exact identifier application number: M017
CAREALL Musle and Joint	MENTHOL	New World Imports, Inc	561cc103-ae88-8f30-e063-6294a90a05c4	2026-07-08	Warnings	Exact identifier application number: M017
HealthWise Medicated Cold Hot	MENTHOL	Veridian Healthcare, LLC	561e1409-d1d8-e35d-e063-6394a90a4d8f	2026-07-08	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