ICY HOT ADVANCED RELIEF- menthol patch 
Chattem, 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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Icy Hot Advanced Relief

Active Ingredient

Menthol 7.5%

Purpose

Topical analgesic

Uses

Temporarily relieves minor pain associated with:

Warnings

For external use only

When using this product

  • use only as directed
  • do not bandage tightly or use with a heating pad
  • avoid contact with eyes and mucous membranes
  • do not apply to wounds or damaged, broken or irritated skin
  • do not use at the same time as other topical analgesics

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

If pregnant of breast feeding,

ask a health 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 and younger: ask a doctor

Inactive ingredients

glyceryl hydrogenated rosinate, hydrated silica, mineral oil, PEG-400, polyisobutene, styrne/isoprene copolymer

Principal Display Panel

ICY HOT®
ADVANCED RELIEF
PAIN RELIEF PATCH
ADVANCED RELIEF at the POINT of PAIN
50% MORE MEDICINE
LONG LASTING RELIEF
FLEXIBLE, NO MESS FABRIC
Easy to Apply and Remove
Contains 4 Patches in 1 Resalable Pouch
3 15/16” x 5 ½” (10 cm x 14 cm) each

ICY HOT®
ADVANCED RELIEF
PAIN RELIEF PATCH
ADVANCED RELIEF at the POINT of PAIN
50% MORE MEDICINE
LONG LASTING RELIEF
FLEXIBLE, NO MESS FABRIC
Easy to Apply and Remove
Contains 4 Patches in 1 Resalable Pouch
3 15/16” x 5 ½” (10 cm x 14 cm) each

ICY HOT ADVANCED RELIEF 
menthol topical analgesic patch
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0805
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 210 mg
Inactive Ingredients
Ingredient Name Strength
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41167-0805-0 1 in 1 CARTON
1 4 in 1 POUCH
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 12/01/2012
Labeler - Chattem, Inc. (003336013)

Revised: 11/2012
Document Id: ad7b463f-93d8-41b6-b251-a9d322a45f67
Set id: 1a100d2a-b0b1-47a2-a1df-5cc394a38b84
Version: 1
Effective Time: 20121109
 
Chattem, Inc.