FDA.reportPublic FDA data

CBDMEDIC Foot and Ankle Pain Relief

Manufacturer
ABACUS HEALTH PRODUCTS, INC. | Aidance Skincare & Topical Solutions, LLC
Effective date
2022-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:42:46

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

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
73096-74773096-747-30

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
WHITE WAX7G1J5DA97FIACT
CLOVE OIL578389D6D0IACT
COTTONSEED OILH3E878020NIACT
EUCALYPTUS OIL2R04ONI662IACT
HEMPTD1MUT01Q7IACT
JOJOBA OIL724GKU717MIACT
PEPPERMINT OILAV092KU4JHIACT
SHEA BUTTERK49155WL9YIACT
SORBIC ACIDX045WJ989BIACT
TEA TREE OILVIF565UC2GIACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB

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
2bc7719e-6589-f86b-e063-6294a90a7158f0ec9c26-29ab-e096-e053-2a95a90a85eb2025-01-01WarningsExact identifier
spl set id: f0ec9c26-29ab-e096-e053-2a95a90a85eb

Reported adverse events (FAERS/openFDA)#

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