GREEN COMPASS REDUCE ROLL-ON PAIN RELIEF- menthol liquid

Green Compass Reduce Roll-On Pain Relief by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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 right away.

DOSAGE & ADMINISTRATION

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

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

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)

INGREDIENTS AND APPEARANCE

GREEN COMPASS REDUCE ROLL-ON PAIN RELIEF 
menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73132-003
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)
HEPTYL GLUCOSIDE (UNII: BU2OC48XBR)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CANNABIS SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
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: 73132-003-60	1 in 1 CARTON	12/03/2020
1		60 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/03/2020

Labeler - Green Compass, Inc. (105963322)