TIDL FULL BODY PAIN RELIEF CRYOTHERAPY SPRAY.- full body pain relief cryotherapy spray. liquid 
The Anthos Group, Inc

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Active Ingredient

Menthol 10.5%

Purpose

Topical Analgesic

Use

Temporary relief from minor aches and pains of muscles and joints associated with arthritis,simple backache,strains and sprains

Warnings

For external use only

Do not use

While smoking or near heat or flame

When Using

·avoid contact with the eyes or mucous membranes
·do not apply to wounds or damaged skin
·do not apply to irritated skin
·do not bandage
·wash hands after use with cool water
·do not use with heating pad or device

Stop Use

if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days

Ask Doctor

if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days

Keep Oot Of Reach Of Children

If accidentally ingested get medical help or contact a Poison Control Center immediately

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:Consult physician

Inactive ingredients

Alcohol Denat, Arnica Montana Flower Extract, Beta-Caryophyllene(Clove), Calendula Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Chamomile Recutita Flower Extract, Dimethyl Sulfone, Echinacea Angustifolia Extract, Ilex Paraguariensis Leaf Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Oil of Wintergreen, Vanilla Extract, Water

Questions

Phone:1(888)778-2986

PRINCIPAL DISPLAY PANEL

1

TIDL FULL BODY PAIN RELIEF CRYOTHERAPY SPRAY. 
full body pain relief cryotherapy spray. liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79740-012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
JUNIPER BERRY (UNII: O84B5194RL)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
CHAMOMILE (UNII: FGL3685T2X)  
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
VANILLA (UNII: Q74T35078H)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
WATER (UNII: 059QF0KO0R)  
CARYOPHYLLENE (UNII: BHW853AU9H)  
ALCOHOL (UNII: 3K9958V90M)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79740-012-0190 mL in 1 BOTTLE; Type 0: Not a Combination Product12/03/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/03/2023
Labeler - The Anthos Group, Inc (117511051)
Establishment
NameAddressID/FEIBusiness Operations
The Anthos Group, Inc117511051manufacture(79740-012) , label(79740-012)

Revised: 12/2023
Document Id: 0baa3842-79e3-9735-e063-6294a90ab4ea
Set id: 0baa3842-79e2-9735-e063-6294a90ab4ea
Version: 1
Effective Time: 20231204
 
The Anthos Group, Inc