Doctor Hoys Pain Relief Gel

Manufacturer: Dynamic Blending Specialists, Inc.
Effective date: 2026-01-02
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:30:59

Label at a glance#

ProductDoctor Hoys Pain Relief Gel

Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)

Label structure9 sections

Indications and uses

Temporary relief of minor aches and pains of muscles and joints due to: simple backache • arthritis • sprains • strains

Dosage and administration

For adults and children 2 years and older: For best results, shake well and apply generously. Use 1 layer for minor pain, 2 layers for medium and 3 layers for severe symptoms • Rub in well and allow to dry between layers (usually 2-3 minutes) • Repeat process up to 4 times daily • for children under 2 years of age: Consult a physician before use.

Label contents#

Full prescribing information#

Active ingredients:

OTC - ACTIVE INGREDIENT SECTION

Menthol (5%)

Camphor (5%)

Purpose:

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains of muscles and joints due to: simple backache • arthritis • sprains • strains

Warnings:

WARNINGS SECTION

• For external use only

• Use as directed

• Avoid contact with eyes or mucus membranes

• Do not apply to open wounds, irritated or damaged skin

Keep Out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately

If pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

• ask a health professional before use

• Discontinue use of this product and consult a physician if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

• Use caution with wrap or heating pad.

Directions:

DOSAGE & ADMINISTRATION SECTION

Inactive ingedients:

INACTIVE INGREDIENT SECTION

Alcohol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Arnica Montana (Arnica Flower) Extract, Biosaccharide Gum-1, Butyrospermum Parkii (Shea) Butter Extract, Ethylhexylglycerin, Euphorbia Cerifera (Candelilla) Wax, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Hydrated Silica, Jojoba Esters, Phenoxyethanol, Polyglyceryl-10 Caprylate/Caprate, SD Alcohol 40-B, Sodium Starch Octenylsuccinate, Tocopherol Acetate, Water, Zanthoxylum Bungeanum Fruit Extract.

75638-010-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label89ml

75638-010-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label177ml

75638-010-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label946ml

75638-010-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1893ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797500	camphor 5 % / menthol 5 % Topical Gel	PSN	4
797500	camphor 0.05 MG/MG / menthol 0.05 MG/MG Topical Gel	SCD	4
797500	camphor 5 % / menthol 5 % Topical Gel	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75638-010-00	2025-02-01	C162847	48780-1	2cef2736-aa78-d83d-e063-dadaa90ab31f	Doctor Hoy's Pain Relief Gel
75638-010-01	2025-02-01	C162847	48780-1	2cef2736-aa78-d83d-e063-dadaa90ab31f	Doctor Hoy's Pain Relief Gel
75638-010-02	2025-02-01	C162847	48780-1	2cef2736-aa78-d83d-e063-dadaa90ab31f	Doctor Hoy's Pain Relief Gel
75638-010-03	2025-02-01	C162847	48780-1	2cef2736-aa78-d83d-e063-dadaa90ab31f	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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

Doctor Hoys Pain Relief Gel
MENTHOL, CAMPHOR (SYNTHETIC)
ALCOHOL
ARNICA MONTANA WHOLE
BIOSACCHARIDE GUM-1
SHEA BUTTER
ETHYLHEXYLGLYCERIN
CANDELILLA WAX
GLYCERIN
HAMAMELIS VIRGINIANA TOP WATER
HYDRATED SILICA
PHENOXYETHANOL
.ALPHA.-TOCOPHEROL ACETATE
WATER
ZANTHOXYLUM BUNGEANUM FRUIT
MENTHOL
CAMPHOR (SYNTHETIC)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75638-010	75638-010-00, 75638-010-01, 75638-010-02, 75638-010-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
ARNICA MONTANA WHOLE	O80TY208ZW	IACT
BIOSACCHARIDE GUM-1	BB4PU4V09H	IACT
SHEA BUTTER	K49155WL9Y	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
CANDELILLA WAX	WL0328HX19	IACT
GLYCERIN	PDC6A3C0OX	IACT
HAMAMELIS VIRGINIANA TOP WATER	NT00Y05A2V	IACT
HYDRATED SILICA	Y6O7T4G8P9	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	IACT
ZANTHOXYLUM BUNGEANUM FRUIT	3CIP16A418	IACT
MENTHOL	L7T10EIP3A	ACTIB
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER	W59H9296ZG	IACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Doctor Hoys Pain Relief Gel	MENTHOL, CAMPHOR (SYNTHETIC)	Dynamic Blending Specialists, Inc.	50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8	2026-01-02	Warnings	Exact identifier ndc (package): 75638-010-01 ndc (package): 75638-010-03 ndc (package): 75638-010-00 ndc (package): 75638-010-02 ndc (product): 75638-010 ndc11 (package): 75638001001 ndc11 (package): 75638001003 ndc11 (package): 75638001000 ndc11 (package): 75638001002 spl id: 4769df6d-225f-5a0d-e063-6394a90af652 spl set id: 50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.