ICY HOT VANISHING SCENT- menthol gel 
Chattem, Inc.

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Icy Hot Vanishing Scent

Drug Facts

Active ingredient

Menthol 2.5%

Purpose

Topical analgesic

Uses

temporarily relieves minor pain associated with:

Warnings

For external use only

When using this product

use only as directed. Read and follow all directions and warnings on this carton.

■ avoid contact with eyes and mucous membranes

rare cases of serious burns have been reported with products of this type

■ do not apply to wounds or damaged, broken or irritated skin

■ do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use

■ a transient burning sensation may occur upon application but generally disappears in several days

avoid applying into skin folds

Stop use and ask a doctor if

■ condition worsens

■ redness is present

■ irritation develops

■ symptoms persist for more than 7 days or clear up and occur again within a few days

■ you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

If pregnant or breast-feeding,

ask a health care professional before use.

Keep out of reach of children.

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

Directions

adults and children over 12 years:

children 12 years or younger: ask a doctor

Inactive ingredients

alcohol denat. (15%), allantoin, aloe barbadensis leaf juice, carbomer, DMDM hydantoin, glycerin, methylparaben, phenoxyethanol, propylparaben, steareth-2, steareth-21, triethanolamine, water

Keep carton as it contains important information.

Close cap tightly after use.

PRINCIPAL DISPLAY PANEL

MENTHOL 2.5%
NEW LOOK

ICYHOT® 
ORIGINAL

VANISHING SCENT
PAIN RELIEVING GEL
Net wt 2.5 oz (70.8 g)

MENTHOL 2.5%
NEW LOOK
ICYHOT® 
ORIGINAL
VANISHING SCENT 
PAIN RELIEVING GEL
Net wt 2.5 oz (70.8 g)

ICY HOT VANISHING SCENT 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0092
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.025 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ALLANTOIN (UNII: 344S277G0Z)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
STEARETH-2 (UNII: V56DFE46J5)  
STEARETH-21 (UNII: 53J3F32P58)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0092-01 in 1 CARTON03/01/2007
171 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/01/2007
Labeler - Chattem, Inc. (003336013)
Establishment
NameAddressID/FEIBusiness Operations
CHATTEM, INC.830410721manufacture(41167-0092)
Establishment
NameAddressID/FEIBusiness Operations
CHATTEM, INC.003336013manufacture(41167-0092)

Revised: 10/2023
Document Id: 1ff6b697-9749-450e-ac12-4b47e9019238
Set id: e2092016-9741-433d-92e6-74bfddadb72c
Version: 6
Effective Time: 20231023
 
Chattem, Inc.