COLD AND HOT NO MESS MEDICATED- menthol, unspecified form spray 
Natural Essentials, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Menthol 16%

Purpose

Topical analgesic

Uses

Warnings

For external use only

Flammable:

  • Do not use while smoking or near heat or flame

Do not apply

  • to wounds or damaged, broken or irritated skin.
  • Do not allow contact with eyes or mucous membranes.

When using this product

  • keep out of eyes
  • do not bandage tightly
  • do not use with a heating pad
  • use only as directed
  • do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120ºF.

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
  • needed for longer than a week

If pregnant or breast-feeding,

  • ask a health professional before use.

Keep out of reach of children and pets.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Glycerin, Propylene Glycol, SDA 40-2 Alcohol, Water.

Principal Display Panel - 4 oz Can Label

CVS
Health

Compare to the
active ingredient in
IcyHot® Pain Relief Spray*

Cold & Hot

MENTHOL 16%

No Mess Medicated Spray

Topical analgesic

SPRAYS AT
ANY ANGLE

NET WT 4 0Z (113 g)

Figure
COLD AND HOT NO MESS MEDICATED 
menthol, unspecified form spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-856
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM160 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66902-856-04118 g in 1 CAN; Type 0: Not a Combination Product10/06/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/06/2020
Labeler - Natural Essentials, Inc. (947484713)
Establishment
NameAddressID/FEIBusiness Operations
NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-856)

Revised: 10/2020
Document Id: 3375fe2d-1510-4aa0-bbc9-8011f3268742
Set id: c2111a11-8aec-418a-81ff-85d41313e484
Version: 1
Effective Time: 20201006
 
Natural Essentials, Inc.