FDA.reportPublic FDA data

Maximum Strength Pain Cream with Pure Hemp Extract

Manufacturer
Royal Labs Natural Cosmetics
Effective date
2021-01-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:56:52

Label at a glance#

ProductMaximum Strength Pain Cream with Pure Hemp Extract
Active ingredientMENTHOL, CAMPHOR (NATURAL), EUCALYPTUS OIL, METHYL SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

Dosage & Administration Section

930mg Hemp Extract (9.3mg per pump)

Warnings Section

For External Use Only. Do not use: on wounds or damaged skin, mouth, genitals or any other mucous membrane, with a heating pad, if condition worsens

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aqua, Butyrospermum Parkii (Shea) Butter, Cetearyl Glucoside, Cetearyl Alcohol, Glyceryl Stearate Citrate, Hemp Extract, Organic Aloe Barbadensis (Aloe Vera) Leaf Juice, Tapioca Starch Modified, Glycerin, Caprylic Capric Triglyceride, Xanthan Gum, Organic Rosmarinus Officinalis (Rosemary) Leaf Extract, Organic Arnica Extract, Glyceryl Caprylate, Caprylhydromamic Acid, Citric Acid.

Indications & Usage

INDICATIONS & USAGE SECTION

Directions: Adults and children 12 years of age and older: Rub onto affected area 3 to 4 times daily; Children under 12 years of age ask a doctor.

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.

Purpose

OTC - PURPOSE SECTION

Uses: For temporary relief of minor aches and pains of muscles and joints associated with: Arthritis, Muscle Strain, Bruises, Sprains, Backache

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Methyl Salicylate 10%

Camphor Bark Oil 3%

Eucalyptus Leaf Oil 2%

Stono Creek Apothocary Maximum Strength Pain Cream with Pure Hemp Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Stono100mlStono100ml

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
69580-10169580-101-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
CETEARYL GLUCOSIDE09FUA47KNAIACT
ROSEMARYIJ67X351P9IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
SHEA BUTTERK49155WL9YIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
WATER059QF0KO0RIACT
ARNICA MONTANAO80TY208ZWIACT
XANTHAN GUMTTV12P4NEEIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
HEMPTD1MUT01Q7IACT
EUCALYPTUS OIL2R04ONI662ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
STARCH, TAPIOCA24SC3U704IIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERINPDC6A3C0OXIACT
METHYL SALICYLATELAV5U5022YACTIB

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
f7aabd60-903e-c39e-e053-6394a90a3b6771d64707-336d-54fc-e053-2a95a90ae6e62023-03-24WarningsExact identifier
spl set id: 71d64707-336d-54fc-e053-2a95a90ae6e6

Reported adverse events (FAERS/openFDA)#

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