CBD PAIN FREEZE SHRINK- 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

HEMP

BOMBS

CBD Pain Freeze Shrink

MENTHOL 4%

1 OZ (28 g)

label

image description

CBD PAIN FREEZE SHRINK 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73423-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CANNABIDIOL (UNII: 19GBJ60SN5)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73423-003-0112 in 1 PACKAGE12/15/202009/30/2025
128 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/15/202009/30/2025
Labeler - Global Widget, LLC (089584863)
Establishment
NameAddressID/FEIBusiness Operations
Global Widget, LLC089584863manufacture(73423-003)
Establishment
NameAddressID/FEIBusiness Operations
Global Widget LLC118504011manufacture(73423-003)

Revised: 12/2023
Document Id: 0c49c820-5cff-e750-e063-6394a90ab42c
Set id: 06f9fd7f-6571-4c9e-bfb9-5d52858c99e7
Version: 4
Effective Time: 20231211
 
Global Widget, LLC