GREEN COMPASS REDUCE PAIN RELIEF WITH MENTHOL- menthol gel

Green Compass Reduce Pain Relief with Menthol by

Drug Labeling and Warnings

Green Compass Reduce Pain Relief with Menthol by is a Otc medication manufactured, distributed, or labeled by Green Compass, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Menthol 5%

PURPOSE

Purpose

Topical Analgesic

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

For external use only.

Do not use

• on wounds or damaged skin
• with a heating pad

When using this product

• avoid contact with the eyes
• do not bandage tightly

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

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

DOSAGE & ADMINISTRATION

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

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

PRINCIPAL DISPLAY PANEL

GREEN COMPASS

REDUCE

PAIN RELIEF GEL

with Menthol

300 mg CBG

ROLL-ON

2 FL OZ (60 mL)

INGREDIENTS AND APPEARANCE

GREEN COMPASS REDUCE PAIN RELIEF WITH MENTHOL 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73132-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
ARNICA MONTANA (UNII: O80TY208ZW)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
CANNABIGEROL (UNII: J1K406072N)
SUNFLOWER OIL (UNII: 3W1JG795YI)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
ALCOHOL (UNII: 3K9958V90M)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EUCALYPTUS OIL (UNII: 2R04ONI662)
LAVENDER OIL (UNII: ZBP1YXW0H8)
WATER (UNII: 059QF0KO0R)
CAMPHOR OIL (UNII: 75IZZ8Y727)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73132-005-60	1 in 1 CARTON	11/01/2023
1		60 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
2	NDC: 73132-005-00	2 mL in 1 PACKET; Type 0: Not a Combination Product	11/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/01/2023

Labeler - Green Compass, Inc. (105963322)