FDA.reportPublic FDA data

CBDMEDIC Arthritis Pain Relief

Manufacturer
AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC
Effective date
2019-03-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:58:52

Label at a glance#

ProductCBDMEDIC Arthritis Pain Relief
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with arthritis.

Dosage and administration

Adults and children 12 years of age and older: massage cream into affected area not more than 3 to 4 times daily. Wash hands with soap and water after use. Children under 12 years of age: ask a doctor.

Label contents#

Full prescribing information#

Active Ingredient and Purpose

OTC - ACTIVE INGREDIENT SECTION

Menthol 4% (External Analgesic)

Uses

OTC - PURPOSE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with arthritis.

Warnings

WARNINGS SECTION

For external use only. Do not use on wounds or damaged skin. When using this product: • avoid contact with eyes or mucous membranes • do not bandage tightly or use with a heating pad. Stop use and ask a doctor if: • condition worsens, or symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation develops.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: massage cream into affected area not more than 3 to 4 times daily. Wash hands with soap and water after use. Children under 12 years of age: ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax (organic), clove oil, cotton seed oil, emulsifying wax, eucalyptus oil, hemp extract (THC-free), jojoba seed oil, peppermint oil, purified water, shea butter, sorbic acid, tea tree oil

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24909-740-482023-01-30C16284748780-1f386c64a-1c86-0266-e053-dadaa90a7c1aCBDMEDIC Arthritis Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24909-740-48CBDMEDIC Arthritis Pain Relief1 in 1 CARTONCREAM11
24909-740-48CBDMEDIC Arthritis Pain Relief48 g in 1 BOTTLE, PUMPCREAM481

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24909-740CBDMEDIC ARTHRITIS PAIN RELIEF (MENTHOL.) CREAM [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]1Legacy NDC, 2 package rows20190318_9f131395-b6c0-41ce-8447-4cde56d96d05.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-74024909-740-48

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
WHITE WAX7G1J5DA97FIACT
CLOVE OIL578389D6D0IACT
COTTONSEED OILH3E878020NIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
EUCALYPTUS OIL2R04ONI662IACT
HEMPTD1MUT01Q7IACT
JOJOBA OIL724GKU717MIACT
PEPPERMINT OILAV092KU4JHIACT
WATER059QF0KO0RIACT
SHEA BUTTERK49155WL9YIACT
SORBIC ACIDX045WJ989BIACT
TEA TREE OILVIF565UC2GIACT

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
6badb356-4530-4d9c-82d3-a085ec56e11c9f131395-b6c0-41ce-8447-4cde56d96d052019-03-12WarningsExact identifier
spl id: 6badb356-4530-4d9c-82d3-a085ec56e11c
spl set id: 9f131395-b6c0-41ce-8447-4cde56d96d05

Reported adverse events (FAERS/openFDA)#

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