CBD Pain Relief

Manufacturer
Global Products Group, LLC
Effective date
2022-01-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:38

Label at a glance#

ProductCBD Pain Relief Clinical Strength Menthol Formula
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

Temporarily relieves foot, ankle and leg pain associated with arthritis muscle aches muscle strains muscle sprains joint pain.

Dosage and administration

Use only as directed Do not use on children under 12 years of age Roll onto affected area no more than four times daily Shake well before each use.

Storage and handling

Call (877) 383-2334. Store in a cool dry place with the cap tightly closed. Note: Because this product contains natural ingredients, color may vary.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Natural Menthol, USP (8.5%)

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves foot, ankle and leg pain associated with arthritis

  • muscle aches
  • muscle strains
  • muscle sprains
  • joint pain.

Warnings

WARNINGS SECTION

For external use only: Flammable: Keep away from excessive heat or open flame

OTC - ASK DOCTOR SECTION

  • Ask a doctor before use if you have sensitive skin or if you are taking any blood thinners

OTC - WHEN USING SECTION

  • When using this product: Do not use on wounds or irritated skin
  • Do not bandage tightly or use with a heating pad
  • Wash hands after use with cool water

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • If pregnant or breastfeeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. If accidentally swallowed, contact a doctor or poison control center immediately

OTC - STOP USE SECTION

  • Stop use and ask a doctor: If condition worsens or if pain persists for more than 7 days, or clears up, then reoccurs within a few days.

Directions

DOSAGE & ADMINISTRATION SECTION

Use only as directed

  • Do not use on children under 12 years of age
  • Roll onto affected area no more than four times daily
  • Shake well before each use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Serrata Extract, Camphor, Carbomer, Chondroitin Sulfate, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Ilex Paraguariensis Extract, Isopropyl Alcohol, Methyl Sulfonylmethane, Peppermint Oil, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Purified Water, Triethanolamine

Other Information

STORAGE AND HANDLING SECTION

Questions or comments?

OTC - QUESTIONS SECTION

Call (877) 383-2334. Store in a cool dry place with the cap tightly closed. Note: Because this product contains natural ingredients, color may vary.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY

HOTWORX®
24 HOUR INFRARED FITNESS STUDIO

planet beach®
spray & spa

PRINCIPAL DISPLAY PANEL - 88 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ROLL ON

CBD
PAIN RELIEF

Clinical Strength Menthol Formula

DISTRIBUTED BY

HOTWORX®
24 HOUR INFRARED FITNESS STUDIO

planet beach®
spray & spa

150mg CBD 3 fl oz (88 mL)

PRINCIPAL DISPLAY PANEL - 88 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 88 mL Bottle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72593-157-122024-01-30C16284748780-11030e365-4e12-111a-e063-dadaa90a10e2CBD Pain Relief Clinical Strength Menthol Formula

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72593-157-12CBD Pain Relief Clinical Strength Menthol Formula88 mL in 1 BOTTLE, WITH APPLICATORGEL882

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72593-157CBD PAIN RELIEF CLINICAL STRENGTH MENTHOL FORMULA (MENTHOL, UNSPECIFIED FORM) GEL [GLOBAL PRODUCTS GROUP, LLC]2Legacy NDC, 1 package rows20220127_2dfeea72-4e24-443c-95e9-b5073b486e86.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72593-15772593-157-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
f9babc71-ef7f-478f-b327-c4aee64ff8c82dfeea72-4e24-443c-95e9-b5073b486e862022-01-25WarningsExact identifier
spl id: f9babc71-ef7f-478f-b327-c4aee64ff8c8
spl set id: 2dfeea72-4e24-443c-95e9-b5073b486e86

Reported adverse events (FAERS/openFDA)#

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