FDA.reportPublic FDA data

CBDMEDIC Foot and Ankle Pain Relief

Manufacturer
AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC
Effective date
2019-12-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:02:30

Label at a glance#

ProductCBDMEDIC Foot and Ankle Pain Relief
Active ingredientCAMPHOR (NATURAL), MENTHOL
Label structure7 sections

Indications and uses

Temporary relief of minor aches and pains of muscles and joints associated with feet, toes and ankles

Dosage and administration

Adults and children 12 years of age and older: • apply to affected area not more than 3 to 4 times daily Children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients and Purpose

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%, Menthol 15% (External Analgesics)

Uses

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains of muscles and joints associated with feet, toes and ankles

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
• symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• excessive skin irritation develops
If pregnant or breast-feeding
ask a health professional before use
Keep out of reach of children
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:
• apply to affected area not more than 3 to 4 times daily
Children under 12 years of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax, shea butter, cottonseed oil, CBD hemp oil, clove oil, eucalyptus oil, jojoba seed oil, sorbic acid, peppermint oil, tea tree oil

Questions?

SPL UNCLASSIFIED SECTION

Call 1-844-422-3633

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24909-747-302023-01-30C16284748780-1f386c649-ccef-0266-e053-dadaa90a7c1aCBDMEDIC Foot and Ankle Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24909-747-30CBDMEDIC Foot and Ankle Pain Relief1 in 1 CARTONSTICK11
24909-747-30CBDMEDIC Foot and Ankle Pain Relief30 g in 1 CYLINDERSTICK301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24909-747CBDMEDIC FOOT AND ANKLE PAIN RELIEF (CAMPHOR AND MENTHOL) STICK [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]1Legacy NDC, 2 package rows20191231_4a023517-4a88-4bf2-9ecf-bc564fc8f1de.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-74724909-747-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB
WHITE WAX7G1J5DA97FIACT
CLOVE OIL578389D6D0IACT
COTTONSEED OILH3E878020NIACT
EUCALYPTUS OIL2R04ONI662IACT
HEMPTD1MUT01Q7IACT
JOJOBA OIL724GKU717MIACT
PEPPERMINT OILAV092KU4JHIACT
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
e207343b-84a9-4554-b832-402a3ac6624e4a023517-4a88-4bf2-9ecf-bc564fc8f1de2019-12-25WarningsExact identifier
spl id: e207343b-84a9-4554-b832-402a3ac6624e
spl set id: 4a023517-4a88-4bf2-9ecf-bc564fc8f1de

Reported adverse events (FAERS/openFDA)#

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