FDA.reportPublic FDA data

DOCTOR HOYS Natural Arnica Boost

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
20
Source
full-release
Hydrated at
2026-06-01 02:18:47

Label at a glance#

ProductDOCTOR HOYS Natural Arnica Boost
Active ingredientARNICA MONTANA
Label structure7 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Warnings: for external use only, 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

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

10% Arnica Montana 1X HPUS

INDICATIONS & USAGE SECTION

Directions: Use by itself or with DOCTOR HOY'S Natural Pain Relief Gel. For adults and children 2 years and older. "Children under 2 years of age: consult a doctor." For best results, apply generously to affected and surrounding areas. Repeat as needed.

Uses: for the temporary relief of minor aches and pains of muscles and joints due to: , inflammation, arthritis, sprains, strains, bruises

INACTIVE INGREDIENT SECTION

Inactive Ingredients: deionized water, hamamelis virginiana (witch hazel extract), isopropyl alcohol, cetyl alcohol, glycerin, tocopheryl acetate (vitamin E), aloe vera, argan oil, calendula oil, chamomile, hyperium Perforatum Extract, safflower oil, tilia cordata flower extract

OTC - PURPOSE SECTION

Uses: for the temporary relief of minor aches and pains of muscles and joints associated with: Inflammation, arthritis, sprains, strains, bruises, Expedites healing, Reduces swelling, Extends relief time, Absorbs quickly, Odorless

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings: for external use only, 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

DOSAGE & ADMINISTRATION SECTION

Directions: Use by itself or with DOCTOR HOY'S Natural Pain Relief Gel. for adults and children 2 years and older. "Children under 2 years of age: consult a doctor." For best results, apply generously to affected and surrounding areas. Repeat as needed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

An image/graphic of the product is included

6oz HPUS Arnica6oz HPUS Arnica

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10842-203-012024-01-30C16284748780-11030e365-65c5-111a-e063-dadaa90a10e2HPUS Arnica Boost
10842-203-022024-01-30C16284748780-11030e365-65c5-111a-e063-dadaa90a10e2HPUS Arnica Boost
10842-203-032024-01-30C16284748780-11030e365-65c5-111a-e063-dadaa90a10e2HPUS Arnica Boost
10842-203-042024-01-30C16284748780-11030e365-65c5-111a-e063-dadaa90a10e2HPUS Arnica Boost
10842-203-062024-01-30C16284748780-11030e365-65c5-111a-e063-dadaa90a10e2HPUS Arnica Boost
10842-203-082024-01-30C16284748780-11030e365-65c5-111a-e063-dadaa90a10e2HPUS Arnica Boost

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10842-203-01DOCTOR HOYS Natural Arnica Boost89 mL in 1 TUBECREAM8920
10842-203-02DOCTOR HOYS Natural Arnica Boost946 mL in 1 JUGCREAM94620
10842-203-03DOCTOR HOYS Natural Arnica Boost1893 mL in 1 JUGCREAM189320
10842-203-04DOCTOR HOYS Natural Arnica Boost6 mL in 1 PACKETCREAM620
10842-203-06DOCTOR HOYS Natural Arnica Boost177 mL in 1 TUBECREAM17720
10842-203-08DOCTOR HOYS Natural Arnica Boost89 mL in 1 BOTTLE, WITH APPLICATORCREAM8920

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10842-203DOCTOR HOYS NATURAL ARNICA BOOST (HPUS ARNICA MONTANA) CREAM [DOCTOR HOY'S, LLC]20Legacy NDC, 6 package rows20221206_9fb2ae79-6bd5-4d18-b24c-63014f699114.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARNICA MONTANA FLOWERACTIVE INGREDIENTOZ0E5Y15PZ8
DIMETHYL SULFONEACTIVE INGREDIENT9H4PO4Z4FT8
ARNICA MONTANA FLOWERACTIVE MOIETYOZ0E5Y15PZ8
DIMETHYL SULFONEACTIVE MOIETY9H4PO4Z4FT8
.ALPHA.-TOCOPHEROL, D-INACTIVE INGREDIENTN9PR3490H98
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X8
ARGAN OILINACTIVE INGREDIENT4V59G5UW9X8
CALENDULA OFFICINALIS FLOWERINACTIVE INGREDIENTP0M7O4Y7YD8
CETEARYL OLIVATEINACTIVE INGREDIENT58B69Q84JO8
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCN8
CHAMOMILEINACTIVE INGREDIENTFGL3685T2X8
HYPERICUM PERFORATUMINACTIVE INGREDIENTXK4IUX8MNB8
JOJOBA OILINACTIVE INGREDIENT724GKU717M8
PANTHENOLINACTIVE INGREDIENTWV9CM0O67Z8
SAFFLOWER OILINACTIVE INGREDIENT65UEH262IS8
TILIA CORDATA WHOLEINACTIVE INGREDIENTW5E5UB44GD8
WATERINACTIVE INGREDIENT059QF0KO0R8
WITCH HAZELINACTIVE INGREDIENT101I4J0U348

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10842-20310842-203-02, 10842-203-01, 10842-203-03, 10842-203-04, 10842-203-06, 10842-203-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CHAMOMILEFGL3685T2XIACT
HYPERICUM PERFORATUMXK4IUX8MNBIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
PANTHENOLWV9CM0O67ZIACT
SAFFLOWER OIL65UEH262ISIACT
CETEARYL OLIVATE58B69Q84JOIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
WITCH HAZEL101I4J0U34IACT
CETYL ALCOHOL936JST6JCNIACT
JOJOBA OIL724GKU717MIACT
ARGAN OIL4V59G5UW9XIACT
ARNICA MONTANAO80TY208ZWACTIB

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 · 21 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNTABLET, COATED / ORAL0.25 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNTABLET, FILM COATED / ORALNAExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNSUSPENSION / AURICULAR (OTIC)1 %w/vExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNSOLUTION / TOPICALNAExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNSUSPENSION / TOPICAL2.01 %w/wExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNAEROSOL / TOPICAL1.16 %w/wExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNAEROSOL, FOAM / RECTAL17 mgExact identifier — unii candidate
20 equally ranked IID candidates
SAFFLOWER OILSAFFLOWER OIL65UEH262ISLOTION / TOPICAL3510 mgExact identifier — unii candidate
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNSUSPENSION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNEMULSION / TOPICALNAExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / VAGINAL200 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNLOTION / TOPICAL1140 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNTABLET, EXTENDED RELEASE / ORAL132 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNTABLET, ORALLY DISINTEGRATING / ORAL9 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNTABLET, FILM COATED, EXTENDED RELEASE / ORAL59 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNAEROSOL, FOAM / TOPICAL82 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNOINTMENT / TOPICAL7 %w/wExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNAEROSOL, FOAM / VAGINAL0.75 %w/wExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNTABLET / ORALNAExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii candidate
20 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCAPSULE, DELAYED RELEASE / ORAL59 mgExact identifier — unii candidate
20 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
ef196dae-5fe1-08b5-e053-2995a90a5f0d9fb2ae79-6bd5-4d18-b24c-63014f6991142022-12-05WarningsExact identifier
spl id: ef196dae-5fe1-08b5-e053-2995a90a5f0d
spl set id: 9fb2ae79-6bd5-4d18-b24c-63014f699114

Reported adverse events (FAERS/openFDA)#

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