Pain Relief Gel

Manufacturer
DOCTOR HOY'S, LLC | Specialty Formulations and Manufacturing LLC | Dynamic Blending Specialists, Inc. | United Laboratories Manufacturing, LLC
Effective date
2022-12-05
Label type
HUMAN OTC DRUG LABEL
Version
19
Source
full-release
Hydrated at
2026-05-31 23:52:04

Label at a glance#

ProductDoctor Hoys Natural Pain Relief
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients      Purpose

Camphor (5%)          External Analgesic        
Menthol (5%)          External Analgesic








OTC - PURPOSE SECTION

Uses:
for the temporary relief of minor aches and pains of muscles and joints due to:
* simple backache * arthritis * sprains * strains * bruises

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings:
* for external use only * do not apply to wounds or damaged skin or bandage tightly * avoid contact with eyes * Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately * if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician * Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use * do not bandage tightly

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

distilled water, hamamelis virginiana (witch hazel extract),
isopropyl alcohol, arnica Montana, oleyl alcohol and
zanthoxylum alatum (scezhuan pepper), Bio-saccharide
Gum -1, glycerin, ammonium acryloyldimethyltaurate/VP
copolymer, beta cyclodextrin, menthol, potassium hydroxide,
mannitol, cellulose chromium, hydroxide green, tocopheryl
acetate (vitamin E), hydroxypropyl methycellulose

DOSAGE & ADMINISTRATION SECTION

Directions:
for adults and children 2 years and older; apply to affected area not more than 3 to 4 times daily. "Children under 2 years of age: consult a doctor." Apply generously to affected and surrounding areas. Rub in well. Use 1 application for minor pain, 2 for medium and 3 applications for severs symptoms. Allow to dry between applications (usually just 2-3 minutes).

INDICATIONS & USAGE SECTION

Directions:

for adults and children 2 years and older; apply to affected area not more than 3 to 4 times daily. "Children under 2 years of age: consult a doctor."  Apply generously to affected and surrounding areas.  Rub in well. Use 1 application for minor pain, 2 for medium and 3 applications for severs symptoms.  Allow to dry between applications (usually just 2-3 minutes).

Uses:

for the temporary relief of minor aches and pains of muscles
and joints due to:

    * simple backache
    * arthritis
    * sprains
    * strains
    * bruises

WARNINGS SECTION

Warnings:

    * for external use only
    * do not apply to wounds or damaged skin or bandage tightly
    * avoid contact with eyes
    * Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately
    * if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician
    * Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use
    * do not bandage tightly

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

An image/jpeg of the container label is included in this section.

 ID: MM1 bottle labelbottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797500camphor 5 % / menthol 5 % Topical GelPSN19
797500camphor 0.05 MG/MG / menthol 0.05 MG/MG Topical GelSCD19
797500camphor 5 % / menthol 5 % Topical GelSY19

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10842-102-01Doctor Hoys Natural Pain Relief237 mL in 1 BOTTLE, DISPENSINGGEL23719
10842-102-02Doctor Hoys Natural Pain Relief1814 mL in 1 JUGGEL181419
10842-102-03Doctor Hoys Natural Pain Relief118 mL in 1 TUBEGEL11819
10842-102-04Doctor Hoys Natural Pain Relief5 mL in 1 PACKETGEL519
10842-102-05Doctor Hoys Natural Pain Relief946 mL in 1 JUGGEL94619
10842-102-08Doctor Hoys Natural Pain Relief89 mL in 1 BOTTLE, WITH APPLICATORGEL8919
10842-102-09Doctor Hoys Natural Pain Relief3785 mL in 1 JUGGEL378519

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10842-102DOCTOR HOYS NATURAL PAIN RELIEF (CAMPHOR, MENTHOL) GEL [DOCTOR HOY'S, LLC]19Legacy NDC, 7 package rows20221206_898f7784-693f-46f6-a9ac-778e0e6aa3b6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9416
MENTHOLACTIVE INGREDIENTL7T10EIP3A6
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9416
MENTHOLACTIVE MOIETYL7T10EIP3A6
ARNICA MONTANAINACTIVE INGREDIENTO80TY208ZW6
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M4163026
WATERINACTIVE INGREDIENT059QF0KO0R6
WITCH HAZELINACTIVE INGREDIENT101I4J0U346

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10842-10210842-102-01, 10842-102-02, 10842-102-04, 10842-102-05, 10842-102-08, 10842-102-09, 10842-102-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL / TOPICAL75 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SPONGE / TOPICAL4 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL, METERED / TOPICAL525 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / AURICULAR (OTIC)6 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302LOTION, AUGMENTED / TOPICAL2070 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / TOPICAL72 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SOLUTION / TOPICAL40 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302TABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SWAB / TOPICAL43.9 %w/wExact identifier — unii candidate
9 equally ranked IID candidates

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ef195bfa-447b-e58b-e053-2a95a90a7073898f7784-693f-46f6-a9ac-778e0e6aa3b62022-12-05WarningsExact identifier
spl id: ef195bfa-447b-e58b-e053-2a95a90a7073
spl set id: 898f7784-693f-46f6-a9ac-778e0e6aa3b6

Reported adverse events (FAERS/openFDA)#

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