Green Compass Reduce Pain Relief Gel with Menthol

Manufacturer
Green Compass, Inc.
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:53:39

Label at a glance#

ProductGreen Compass Reduce Pain Relief with Menthol
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Menthol 5%

OTC - PURPOSE SECTION

Purpose

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses

For temporary relief of minor aches and pains of muscles and joints.

WARNINGS SECTION

Warnings

For external use only.

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • with a heating pad

OTC - WHEN USING SECTION

When using this product

  • avoid contact with the eyes
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days
  • condition clears up and occurs again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

DOSAGE & ADMINISTRATION SECTION

Directions

  • use as directed
  • 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 INGREDIENT SECTION

Inactive ingredients

Alcohol, aqua (water), arnica montana (arnica) flower extract, Caprylhydroxamic Acid, Cinnamomum Camphora (Camphor) Bark Oil, eucalyptus globulus leaf oil, glyceryl caprylate, helianthus annuus (sunflower) seed oil, hemp flower extract (cannabigerol), hydroxyethylcellulose, lavandula angustifolia (lavender) flower oil, organic aloe barbadensis leaf juice, xanthan gum.

SPL UNCLASSIFIED SECTION

Distributed By:

Green Compass, LLC.

1121 Military Cutoff Rd., Ste C339

Wilmington, NC 28405 USA

Do not use if tamper evident seal is broken or missing.

1-833-33-MYCBD

support@greencompassglobal.com

greencompassglobal.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GREEN COMPASS

REDUCE

PAIN RELIEF GEL

with Menthol

300 mg CBG

ROLL-ON

2 FL OZ (60 mL)

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73132-005-00Green Compass Reduce Pain Relief with Menthol2 mL in 1 PACKETGEL22
73132-005-60Green Compass Reduce Pain Relief with Menthol60 mL in 1 BOTTLE, WITH APPLICATORGEL602
73132-005-60Green Compass Reduce Pain Relief with Menthol1 in 1 CARTONGEL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73132-005GREEN COMPASS REDUCE PAIN RELIEF WITH MENTHOL (MENTHOL) GEL [GREEN COMPASS, INC.]2Current NDC, 3 package rows20250126_0a0c212e-ae5d-8505-e063-6394a90af622.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73132-00573132-005-60, 73132-005-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Green Compass Reduce Pain Relief with MentholMENTHOLGreen Compass, Inc.0a0c212e-ae5d-8505-e063-6394a90af6222025-01-01WarningsExact identifier
ndc (package): 73132-005-00
ndc (package): 73132-005-60
ndc (product): 73132-005
ndc11 (package): 73132000500
ndc11 (package): 73132000560
spl id: 2c7baad3-2add-ba3f-e063-6294a90a3bb3
spl set id: 0a0c212e-ae5d-8505-e063-6394a90af622

Reported adverse events (FAERS/openFDA)#

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