Green Compass Reduce Roll-On Pain Relief

Manufacturer
Green Compass, Inc.
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:54:05

Label at a glance#

ProductGreen Compass Reduce Roll-On Pain Relief
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Label contents#

Full prescribing information#

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 right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • 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

Water (Aqua), Full Spectrum Hemp Flower Extract, Hydroxyethylcellulose, Ethyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Heptyl Glucoside, Organic Aloe Barbadensis Leaf Juice, Tocopherol, Arnica Montana (Arnica) Flower Extract, Cinnamomom Camphora (Camphor) Bark Oil, Lavandula Angustifolia (Lavender) Flower Oil, Xanthan Gum, Glyceryl Caprylate, Caprylhydroxamic Acid.

SPL UNCLASSIFIED SECTION

Distributed By:

Green Compass, Inc.

1121 Military Cutoff Rd., Ste C339

Wilmington, NC 28405 USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REDUCE

ROLL-ON PAIN RELIEF

WITH MENTHOL AND 300 mg FULL SPECTRUM HEMP FLOWER EXTRACT

GREEN COMPASS

2 FL OZ (60 mL)

GRC 176 Reduce Roll-on FinalGRC 176 Reduce Roll-on Final

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73132-003-602025-02-01C16284748780-12cef2736-8b55-d83d-e063-dadaa90ab31fGreen Compass Reduce Roll-On Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73132-003-60Green Compass Reduce Roll-On Pain Relief60 mL in 1 BOTTLE, WITH APPLICATORLIQUID603
73132-003-60Green Compass Reduce Roll-On Pain Relief1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73132-003GREEN COMPASS REDUCE ROLL-ON PAIN RELIEF (MENTHOL) LIQUID [GREEN COMPASS, INC.]3Current NDC, Legacy NDC, 2 package rows20250131_b5916aa2-428c-5637-e053-2995a90a08b0.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
73132-00373132-003-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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 Roll-On Pain ReliefMENTHOLGreen Compass, Inc.b5916aa2-428c-5637-e053-2995a90a08b02025-01-01WarningsExact identifier
ndc (package): 73132-003-60
ndc (product): 73132-003
ndc11 (package): 73132000360
spl id: 2c7bc7eb-b086-ef56-e063-6394a90a6f42
spl set id: b5916aa2-428c-5637-e053-2995a90a08b0

Reported adverse events (FAERS/openFDA)#

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