CBD GLOBAL FREEZE- methyl salicylate, menthol, camphor spray

CBD Global Freeze by

Drug Labeling and Warnings

CBD Global Freeze by is a Otc medication manufactured, distributed, or labeled by Cosmetic Specialty Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Incredients

Methyl Salicylate 30%

Menthol 10%

Camphor Oil 4%

Purpose

Topical analgesi

Uses

temporarily relieves minor pain associated with: arthritis simple backache muscle strains sprains bruises cramps

Warnings

for external use only

WHEN USING

When using this prodcut use only as directed avoid contact with eyes or mucous membranes do not apply to wounds or damaged skin do not bandage tightly

STOP USE

Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness is present irritation develeps

KEEP OUT OF REACH OF CHILDREN

If pregnant or breast-feeding, ask a health professional before use.

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

Directions:

Adults and children over 2 years: apply generously to affected area massage into painful area until throughly absorbed into skin repeat as necessary, but no more than 4 time daily

Children 2 years or younger: ask a doctor

Inactive ingredients

Industrial Hemp CBD(200mg), CBG(10mg), CBN(10mg), Isopropyl Alcohol

Package Label

INGREDIENTS AND APPEARANCE

CBD GLOBAL FREEZE 
methyl salicylate, menthol, camphor spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58133-954
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g  in 100 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	30 g  in 100 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CANNABIDIOL (UNII: 19GBJ60SN5)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CANNABINOL (UNII: 7UYP6MC9GH)
CANNABIGEROL (UNII: J1K406072N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58133-954-02	25 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/28/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/28/2022

Labeler - Cosmetic Specialty Labs, Inc. (032973000)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmetic Specialty Labs, Inc.		032973000	manufacture(58133-954) , pack(58133-954) , label(58133-954)