Doctor Hoy's Arnica Boost Recovery Cream

Manufacturer
Dynamic Blending Specialists, Inc.
Effective date
2026-01-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:36:36

Label at a glance#

ProductDoctor Hoys Arnica Boost Recovery
Active ingredientARNICA MONTANA
Label structure8 sections

Indications and uses

Temporary relief of minor aches and pains associated with: scrapes • bruising • joints • sprains • inflammation

Dosage and administration

• For adults and children 2 years and older: Apply generously to affected and surrounding areas  • Repeat use as needed  • For children under 2 years of age: Consult a physician before use.

Label contents#

Full prescribing information#

Active ingredients:

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 1X HPUS (5%)

Purpose:

OTC - PURPOSE SECTION

Anit-inflammatory

Uses:

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains associated with: scrapes • bruising • joints • sprains • inflammation

Warnings:

WARNINGS SECTION

• For external use only

• Use as directed 

• Avoid contact with eyes

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.

Directions:

DOSAGE & ADMINISTRATION SECTION

• For adults and children 2 years and older: Apply generously to affected and surrounding areas 

• Repeat use as needed 

• For children under 2 years of age: Consult a physician before use.

Inactive ingedients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Anthemis Nobilis (Chamomile) Flower Oil, Argania Spinosa Kernel (Argan) Oil, Calendula Officinalis, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Olivate, Cetyl Alcohol, DL Panthenol, Glycerin, Glyceryl Stearate, Hamamelis Virginiana (Witch Hazel), Hypericum Perforatum (St. Johns Wort), MSM (Methyl Sulfonyl Methane), Phenoxyethanol(and) Ethylhexylglycerin, Simmondsia Chinensis (Jojoba) Seed Oil, Squalane, Stearic Acid, Triethanolamine, Tocopherol, Water.

75638-009-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 89mlLabel 89ml

75638-009-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 177mlLabel 177ml

75638-009-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 946mlLabel 946ml

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75638-009-00Doctor Hoys Arnica Boost Recovery89 mL in 1 TUBEGEL893
75638-009-01Doctor Hoys Arnica Boost Recovery177 mL in 1 TUBEGEL1773
75638-009-02Doctor Hoys Arnica Boost Recovery946 mL in 1 TUBEGEL9463

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75638-00975638-009-00, 75638-009-01, 75638-009-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Doctor Hoys Arnica Boost RecoveryARNICA MONTANADynamic Blending Specialists, Inc.7e639152-b423-4db8-9078-b5c929d6a07d2026-01-02WarningsExact identifier
ndc (package): 75638-009-01
ndc (package): 75638-009-02
ndc (package): 75638-009-00
ndc (product): 75638-009
ndc11 (package): 75638000901
ndc11 (package): 75638000902
ndc11 (package): 75638000900
spl id: 4769bbc4-c164-6de3-e063-6294a90a225f
spl set id: 7e639152-b423-4db8-9078-b5c929d6a07d

Reported adverse events (FAERS/openFDA)#

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