PainPatrol CBD Professional Pain Relief

Manufacturer
SmartScience Laboratories, Inc.
Effective date
2019-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:18

Label at a glance#

ProductPainPatrol CBD Professional Pain Relief
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.

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 is you have sensitive skin or if you are taking any blood thinners,

When using this product

OTC - WHEN USING SECTION

Do not use on wounds or irritated skin

  • Do not bandage tightly or usewith a heating pad
  • Wash hands after use with cool water

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • If pregnant or breast feeding, 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 Extract, Boswellia Serrata Extract, Camphor, Cannabis Sativa Seed Oil (Hemp Derived), Carbomer, Chondroitin Sulfate, Glucosamine Sulfate, Glycerin, Ilex Paraguarensis Extract, Isopropyl Alcohol, Methyl Paraben, Methylsulfonylmethane, Peppermint Oil, Polysorbate 20, Propylene Glycol, Purified Water,Triethanolamine.

Other Information

SPL UNCLASSIFIED SECTION

Questions or comments?

OTC - QUESTIONS SECTION

Call (877) 383-2334.

STORAGE AND HANDLING SECTION

Store in a cool dry place with the cap tightly closed. Note: Because this product contains natural ingredients, color may vary.

SPL UNCLASSIFIED SECTION

Manufactured by: SmartScience Laboratories, Inc.
13760 Reptron Blvd., Tampa, FL 33626

PRINCIPAL DISPLAY PANEL - 88 ML Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clinical Strength Menthol Formula

PainPatrol™
CBD
Professional Pain Relief

Pain Relief for arthritis, joints and muscles
Also contains Glucosamine • Chondroitin • Arnica • Boswellia

150mg CDB
No Mess Applicator.
3FL OZ (88ML)

Principal Display Panel - 88 ML Bottle Label
Principal Display Panel - 88 ML Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64479-201-112024-01-30C16284748780-11030e365-030a-111a-e063-dadaa90a10e2PainPatrol™ CBD Professional Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64479-201-11PainPatrol CBD Professional Pain Relief88 mL in 1 BOTTLE, WITH APPLICATORGEL881

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64479-201PAINPATROL CBD PROFESSIONAL PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) GEL [SMARTSCIENCE LABORATORIES, INC.]1Legacy NDC, 1 package rows20190420_ecc8f4c5-2ccb-4d54-a3c1-b9b8d0ad8a50.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64479-20164479-201-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
c04c298d-b275-4a45-8bc3-4f53dff5b5a1ecc8f4c5-2ccb-4d54-a3c1-b9b8d0ad8a502019-04-08WarningsExact identifier
spl id: c04c298d-b275-4a45-8bc3-4f53dff5b5a1
spl set id: ecc8f4c5-2ccb-4d54-a3c1-b9b8d0ad8a50

Reported adverse events (FAERS/openFDA)#

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