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 21 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
New Terocin	METHYL SALICYLATE, CAPSAICIN, AND MENTHOL	ASCLEMED USA INC.	68dc0231-3364-448b-bde9-f19fa122c765	2026-05-05	Warnings	Exact identifier application number: M017
Lidocaine 4% Patch	LIDOCAINE 4%	SOLA Pharmaceuticals	c31957dd-edea-ce98-e053-2a95a90a9c2d	2026-05-05	Warnings	Exact identifier application number: M017
Biofreeze Triple Target Gel	CAMPHOR, CAPSAICIN, MENTHOL	Reckitt Benckiser LLC	511852c8-7428-3234-e063-6394a90a5bc2	2026-05-05	Warnings	Exact identifier application number: M017
5Kind DMSO Pain Relieving	CAMPHOR (SYNTHETIC)	5Kind Trading LTD	62b55114-47f4-473a-8406-78238c3c1fa2	2026-05-04	Warnings	Exact identifier application number: M017
Zinc Oxide with Menthol and White Petrolatum	MENTHOL, ZINC OXIDE, WHITE PETROLATUM	Aldermed Inc.	f993fc0a-bd80-4345-a948-65ac03f910e2	2026-05-04	Warnings	Exact identifier application number: M017
EVERLIT CARE PRODUCTS BURN RELIEF	LIDOCAINE HYDROCHLORIDE	EVERLIT GLOBAL INC.	d7ec5720-4d1f-4943-ae36-c7d6acbae7d7	2026-05-04	Warnings	Exact identifier application number: M017
EVERLIT CARE PRODUCTS BURN RELIEF	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	5371dae4-ea63-46cc-ac26-5418f359c63e	2026-05-04	Warnings	Exact identifier application number: M017
EVERLIT CARE BURN	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	a2cf1726-3dc9-4624-b898-ac91fb4cbdb2	2026-05-04	Warnings	Exact identifier application number: M017
FIRSTAR BURN	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	186343c5-2e71-49c4-8d64-5fb3131239fa	2026-05-04	Warnings	Exact identifier application number: M017
Feminine Anti Itch Cream	BENZOCAINE,RESORCINOL	TRIFECTA PHARMACEUTICALS USA LLC	50c3acbf-b873-908a-e063-6294a90a66b7	2026-05-01	Warnings	Exact identifier application number: M017
24 7 Relief and Recovery Pain Relieving	MENTHOL, UNSPECIFIED FORM	Triplicare Inc	53ca807b-3ec2-4b5e-aa5a-6dcb756bb423	2026-04-30	Warnings	Exact identifier application number: M017
FIRST AID BURN	LIDOCAINE HYDROCHLORIDE,BENZALKONIUM CHLORIDE	4 Visions LLC	50b1351d-72dd-e0c9-e063-6294a90ac743	2026-04-30	Warnings	Exact identifier application number: M017
TheraCare Flexible Pain Relieving	LIDOCAINE	Veridian Healthcare	4f108002-2cae-0671-e063-6294a90ab6cf	2026-04-30	Warnings	Exact identifier application number: M017
Pain Relief Gel Roll On	MENTHOL	Trifecta Pharmaceuticals USA	50b1a420-d5cd-6d61-e063-6294a90a0451	2026-04-30	Warnings	Exact identifier application number: M017
Dr. Numb	LIDOCAINE AND BENZETHONIUM CHLORIDE CREAM	Shinpharma Inc	d8cdccdb-775b-4970-a6ea-50b62df221d6	2026-04-30	Warnings	Exact identifier application number: M017
hydrocortisone	HYDROCORTISONE	Padagis Israel Pharmaceuticals Ltd	2dc7f76f-f9ad-46ba-8b41-952e1c15f052	2026-04-29	Warnings	Exact identifier application number: M017
anti itch	HYDROCORTISONE	HyVee Inc	e1db3641-2e83-4fec-8394-98d0d876ce0d	2026-04-29	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Roll On	MENTHOL, METHYL SALICYLATE	PT. EAGLE INDO PHARMA	50805eee-33b3-86bd-e063-6294a90a77d8	2026-04-28	Warnings	Exact identifier application number: M017
FixMySkin Healing Balm Vanilla Flavor	HYDROCORTISONE	Lovely Skin, Inc.	52f7a561-a0b5-4562-a588-d74fd874b83a	2026-04-28	Warnings	Exact identifier application number: M017
Blue Star Medicated	CAMPHOR	Focus Consumer Healthcare, LLC	56df008e-a23b-4870-e054-00144ff8d46c	2026-04-27	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