Menthol - Aidance Skincare & Topical Solutions, LLC

Manufacturer
Aidance Skincare & Topical Solutions, LLC
Effective date
2016-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:39

Label at a glance#

ProductCBD Clinic - Moderate Muscle and Joint Pain Relief
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

Temporarily relieves minor aches and pain of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

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

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

Purpose

OTC - PURPOSE SECTION

Menthol - Topical Anesthetic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pain of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

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 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: 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 (organic), hemp extract, clove oil, cotton seed oil, emulsifying wax, eucalyptus citrodora oil, jojoba seed oil, magnesium oxide, peppermint oil, purified water, shea butter, silver oxide, sorbic acid, tea tree oil, zinc oxide.

PRINCIPAL DISPLAY PANEL - 44g Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MODERATE MUSCLE & JOINT PAIN RELIEF

with 4% Menthol

CBD CLINIC

Revolutionary Pain Relief

Level 3 PROFESSIONAL SERIES Cream Net WT 44 grams

Jar LabelJar Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24909-703-442021-01-29C16284748780-1ba0f9c33-2c13-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24909-703-44CBD Clinic - Moderate Muscle and Joint Pain Relief44 g in 1 JARCREAM441

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24909-703CBD CLINIC - MODERATE MUSCLE AND JOINT PAIN RELIEF (MENTHOL) CREAM [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]1Legacy NDC, 1 package rows20160728_c99b7504-ec1b-4e3e-950b-e2ef42649b00.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-70324909-703-44

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
1e7a9252-681e-4294-b01e-bb0b245cfc2ac99b7504-ec1b-4e3e-950b-e2ef42649b002016-07-14WarningsExact identifier
spl id: 1e7a9252-681e-4294-b01e-bb0b245cfc2a
spl set id: c99b7504-ec1b-4e3e-950b-e2ef42649b00

Reported adverse events (FAERS/openFDA)#

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