Label: ICY HOT ARM NECK LEG AND SMALL AREAS- menthol patch
ICY HOT BACK AND LARGE AREAS- menthol patch
ICY HOT XL BACK AND LARGE AREAS- menthol patch

  • NDC Code(s): 41167-0073-8, 41167-0083-2, 41167-0084-1, 41167-0843-1, view more
    41167-0843-2, 41167-0843-7, 41167-0847-1, 41167-0847-2
  • Packager: Chattem, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 27, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Icy Hot® - Medicated Patch

    ARM, NECK & LEG & SMALL AREAS

  • Active Ingredient

    Menthol 5%

  • Purpose

    Topical analgesic

  • Uses

    • temporarily relieves minor pain associated with:
      • arthritis
      • simple backache
      • bursitis
      • tendonitis
      • muscle strains
      • sprains
      • bruises
      • cramps
  • 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 skin, broken or irritated skin 
    • do not bandage tightly or apply local heat (such as heating pads) to the area of use
    • a transient burning sensation may occur upon application but generally disappears in several days

    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 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.

    • remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle
    • carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area
    • once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area
    • apply one patch to affected area
    • wear one Icy Hot Patch up to 8 hours
    • repeat as necessary, but no more than 3 times daily

    children 12 years or younger: ask a doctor

  • Inactive Ingredients

    aluminum hydroxide, cellulose gum, glycerin, isopropyl myristate, methyl acrylate/2-ethylhexyl acrylate copolymer, nonoxynol-30, polyacrylic acid, polysorbate 80, sodium polyacrylate, sorbitan sesquioleate, starch/acrylic acid graft copolymer sodium salt, talc, tartaric acid, titanium dioxide, water 

    KEEP CARTON AS IT CONTAINS IMPORTANT INFORMATION FOR USAGE OF THE PRODUCT.

    Distributed by Chattem, Inc.
    P.O. Box 2219
    Chattanooga, TN 37409-0219 USA 
    ©2020 www.icyhot.com  
    Made in Japan.


    Icy Hot® - Medicated Patch

    BACK & LARGE AREAS

  • Active Ingredient

    Menthol 5%

  • Purpose

    Topical analgesic

  • Uses

    • temporarily relieves minor pain associated with:
      • arthritis
      • simple backache
      • bursitis
      • tendonitis
      • muscle strains
      • sprains
      • bruises
      • cramps
  • 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 skin, broken or irritated skin 
    • do not bandage tightly or apply local heat (such as heating pads) to the area of use
    • a transient burning sensation may occur upon application but generally disappears in several days

    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 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.

    • remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle
    • carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area
    • once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area
    • apply one patch to affected area
    • wear one Icy Hot Patch up to 8 hours
    • repeat as necessary, but no more than 3 times daily

    children 12 years or younger: ask a doctor

  • Inactive Ingredients

    aluminum hydroxide, cellulose gum, glycerin, isopropyl myristate, methyl acrylate/2-ethylhexyl acrylate copolymer, nonoxynol-30, polyacrylic acid, polysorbate 80, sodium polyacrylate, sorbitan sesquioleate, starch/acrylic acid graft copolymer sodium salt, talc, tartaric acid, titanium dioxide, water 

    KEEP CARTON AS IT CONTAINS IMPORTANT INFORMATION FOR USAGE OF THE PRODUCT.

    Distributed by Chattem, Inc.
    P.O. Box 2219
    Chattanooga, TN 37409-0219 USA
    ©2020 www.icyhot.com
    Made in Japan.


    Icy Hot® - Medicated Patch

    XL BACK & LARGE AREAS

  • Active Ingredient

    Menthol 5%

  • Purpose

    Topical analgesic

  • Uses

    • temporarily relieves minor pain associated with:
      • arthritis
      • simple backache
      • bursitis
      • tendonitis
      • muscle strains
      • sprains
      • bruises
      • cramps
  • 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 skin, broken or irritated skin 
    • do not bandage tightly or apply local heat (such as heating pads) to the area of use
    • a transient burning sensation may occur upon application but generally disappears in several days

    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 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.

    • remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle
    • carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area
    • once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area
    • apply one patch to affected area
    • wear one Icy Hot Patch up to 8 hours
    • repeat as necessary, but no more than 3 times daily

    children 12 years or younger: ask a doctor

  • Inactive Ingredients

    aluminum hydroxide, cellulose gum, glycerin, isopropyl myristate, methyl acrylate/2-ethylhexyl acrylate copolymer, nonoxynol-30, polyacrylic acid, polysorbate 80, sodium polyacrylate, sorbitan sesquioleate, starch/acrylic acid graft copolymer sodium salt, talc, tartaric acid, titanium dioxide, water 

    KEEP CARTON AS IT CONTAINS IMPORTANT INFORMATION FOR USAGE OF THE PRODUCT.

    Distributed by Chattem, Inc.
    P.O. Box 2219
    Chattanooga, TN 37409-0219 USA
    ©2020 www.icyhot.com
    Made in Japan.



  • Principal Display Panel

    ICY HOT®  
    ORIGINAL
    Pain Relief Patch
    Menthol 5%
    ICY to DULL, HOT to RELAX
    Wear for up to 8 Hours
    Small Patch
    3-1/8” x 4-5/8” (8 cm x 12 cm) each
    ARM. NECK & LEG PATCH
    Contains 5 Patches in 1 Resealable Pouch

    ICY HOT® ORIGINAL Pain Relief Patch Menthol 5% ICY to DULL, HOT to RELAX Wear for up to 8 Hours Small Patch 3-1/8” x 4-5/8” (8 cm x 12 cm) each ARM. NECK & LEG PATCH Contains 5 Patches in 1 Resealable Pouch

  • Principal Display Panel

    ICY HOT®  
    ORIGINAL
    Pain Relief Patch
    Menthol 5%
    ICY to DULL, HOT to RELAX
    Wear for up to 8 Hours
    LARGE PATCH
    3-15/16” x 7-13/16” (10 cm x 20 cm) each
    Contains 5 Patches In 1 Resealable Pouch

    Principal Display Panel ICY HOT® ORIGINAL Pain Relief Patch Menthol 5% ICY to DULL, HOT to RELAX Wear for up to 8 Hours LARGE PATCH 3-15/16” x 7-13/16” (10 cm x 20 cm) each Contains 5 Patches In 1 Resealable Pouch

  • Principal Display Panel

    ICY HOT®  
    ORIGINAL
    Pain Relief Patch
    Menthol 5%
    ICY to DULL, HOT to RELAX
    Wear for up to 8 Hours
    XL PATCH
    5-1/2” x 9-3/4” (14 cm x 25 cm) each
    Contains 3 Patches In 1 Resealable Pouch

    Principal Display Panel ICY HOT® ORIGINAL Pain Relief Patch Menthol 5% ICY to DULL, HOT to RELAX Wear for up to 8 Hours XL PATCH 5-1/2” x 9-3/4” (14 cm x 25 cm) each Contains 3 Patches In 1 Resealable Pouch

  • Principal Display Panel

    ICY HOT®  
    ORIGINAL
    Pain Relief Patch

    Principal Display Panel ICY HOT® ORIGINAL Pain Relief Patch

  • Principal Display Panel

    ICY HOT®  
    ORIGINAL
    Pain Relief Patch
    Menthol 5%

    Principal Display Panel ICY HOT® ORIGINAL Pain Relief Patch Menthol 5%

  • INGREDIENTS AND APPEARANCE
    ICY HOT ARM NECK LEG AND SMALL AREAS 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0084
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL205.50 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL ACRYLATE (UNII: WC487PR91H)  
    ETHYLHEXYL ACETATE (UNII: 2C7K8OA8SB)  
    NONOXYNOL-30 (UNII: JJX07DG188)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    TALC (UNII: 7SEV7J4R1U)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0084-11 in 1 CARTON11/01/2000
    15 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/01/2000
    ICY HOT BACK AND LARGE AREAS 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0843
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL428.50 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL ACRYLATE (UNII: WC487PR91H)  
    ETHYLHEXYL ACETATE (UNII: 2C7K8OA8SB)  
    NONOXYNOL-30 (UNII: JJX07DG188)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    TALC (UNII: 7SEV7J4R1U)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0843-11 in 1 CARTON03/01/2003
    15 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:41167-0843-73 in 1 CARTON03/01/2003
    25 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:41167-0843-21 in 1 CARTON03/01/2003
    36 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/2003
    ICY HOT XL BACK AND LARGE AREAS 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0847
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL750.00 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    ETHYLHEXYL ACETATE (UNII: 2C7K8OA8SB)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL ACRYLATE (UNII: WC487PR91H)  
    NONOXYNOL-30 (UNII: JJX07DG188)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    TALC (UNII: 7SEV7J4R1U)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0847-11 in 1 CARTON12/01/2007
    13 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:41167-0847-21 in 1 CARTON03/10/2017
    24 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/01/2007
    ICY HOT BACK AND LARGE AREAS 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0073
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL428.50 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    ETHYLHEXYL ACETATE (UNII: 2C7K8OA8SB)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL ACRYLATE (UNII: WC487PR91H)  
    NONOXYNOL-30 (UNII: JJX07DG188)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    TALC (UNII: 7SEV7J4R1U)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0073-82 in 1 CARTON03/01/2003
    15 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/2003
    ICY HOT BACK AND LARGE AREAS 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0083
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL428.50 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    ETHYLHEXYL ACETATE (UNII: 2C7K8OA8SB)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL ACRYLATE (UNII: WC487PR91H)  
    NONOXYNOL-30 (UNII: JJX07DG188)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    TALC (UNII: 7SEV7J4R1U)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0083-21 in 1 POUCH; Type 0: Not a Combination Product03/01/2003
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/2003
    Labeler - Chattem, Inc. (003336013)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!