ARTHRITIS HOT- menthol and methyl salicylate cream 
Chattem, Inc.

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Arthritis Hot

Drug Facts

Active ingredients

Menthol 10%

Methyl salicylate 15%

Purpose

Topical analgesic

Uses

temporarily relieves minor pain associated with:

Warnings

For external use only

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

When using this product

  • use only as directed
  • do not bandage tightly or use with a heating pad
  • avoid contact with eyes or mucous membranes
  • do not apply to wounds or damaged, broken or irritated skin

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 develops

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

carbomer, cetyl esters, diisopropyl adipate, emulsifying wax, oleth-3 phosphate, stearic acid, triethanolamine, water (283-085)

PRINCIPAL DISPLAY PANEL

ARTHRITIS HOT
deep penetrating Pain Relief Crème
NET WT 3 OZ (85g)

PRINCIPAL DISPLAY PANEL
ARTHRITIS HOT
deep penetrating Pain Relief Crème
NET WT 3 OZ (85g)

ARTHRITIS HOT 
menthol and methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0600
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE15 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CETYL ESTERS WAX (UNII: D072FFP9GU)  
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0600-31 in 1 CARTON12/01/1998
185 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/01/1998
Labeler - Chattem, Inc. (003336013)

Revised: 10/2023
Document Id: b1ee473f-ed30-4080-968a-1d3aa36be122
Set id: cc57b9b6-8ba5-4ff3-a5df-97d8f5b1bebd
Version: 5
Effective Time: 20231023
 
Chattem, Inc.