CBD CRYOTHERAPY PAIN RELIEF by Global Widget, LLC / Global Widget LLC Drug Facts

Drug Details [pdf]

CBD CRYOTHERAPY PAIN RELIEF- menthol gel
Global Widget, LLC

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Drug Facts

Active Ingredients

Menthol USP 4%

Purpose

Topical Analgesic

Uses

For the temporary relief of pain

Warnings

FOR EXTERNAL USE ONLY

Do not use:

On eyes or on mucous membranes
On wounds, damaged or irritated skin
If you are allergic to Menthol or any of the ingredients listed below

When using this product:

Use only as directed
Do not bandage or cover with any type of wrap except clothing
Do not use with heating pad or devices, or apply external heat

Stop use and ask a doctor if

Localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
Conditions worsen
Symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breastfeeding: Do not use this product.

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

Directions

Adults 18 years & over rub a thin layer into affected areas up to 4 times daily.

Wash hands after application.

Other Information:

Store in cool, dry place away from direct sunlight

Do not use if seal is broken or not present

Inactive Ingredients

Water, Isopropyl Alcohol, Carbomer, Pure CBD Extract, Triethanolamine

Distributed by

Global Widget, LLC

8419 Sunstate Street, Tampa, FL 33634

Principal Display Panel

NATURE'S

SCRIPT

CBD Cryotherapy Pain Relief Gel

MENTHOL 4%

1 OZ (28 g)

label

image description

CBD CRYOTHERAPY PAIN RELIEF
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73423-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	40 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CANNABIDIOL (UNII: 19GBJ60SN5)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 73423-002-01	12 in 1 PACKAGE	12/17/2020	04/30/2025
1		28 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	12/17/2020	04/30/2025

Labeler - Global Widget, LLC (089584863)

Name	Address	ID/FEI	Business Operations
Establishment
Global Widget, LLC		089584863	manufacture(73423-002)

Name	Address	ID/FEI	Business Operations
Establishment
Global Widget LLC		118504011	manufacture(73423-002)

Revised: 12/2023

Document Id: 0c49a83c-cdf7-3f85-e063-6294a90a34e1

Set id: e41e2811-f1c5-46f5-8124-5d66c3b10e6b

Version: 4

Effective Time: 20231211