Available Formats

• Active Ingredient

  Menthol 5.0%
  

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• Purpose

  Topical Analgesic

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• Uses

  temporarily relieves minor pain associated with

  • arthritis
  • simple backache
  • bursitis
  • tendonitis
  • muscle strains
  • sprains
  • bruises
  • cramps

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• Warnings

  For external use only
  

  When using this product

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

  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 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.

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• Directions

  Adults and children over 12 years:

  • carefully remove backing from patch
  • apply one patch to affected area
  • repeat as necessary, but no more than 4 times daily

  Children 12 years or younger: ask a doctor

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• Inactive ingredients

  Acrylic Acid, Aluminum Hydroxide, Carmellose sodium, 2-Ethylhexyl Acrylate, Glycerin, Isopropyl Myristate, Methyl Acrylate, Nonoxymol-30, Sodium Polyacrylate, Polyacrylic Acid, Polysorbate 80, Purified Water, Sorbitan Sesquioleate, Starch, Talc, Tartaric acid, Titanium Dioxide

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• package label

  QC Cold and Hot Patch

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• INGREDIENTS AND APPEARANCE

  QC COLD AND HOT PAIN RELIEF  menthol patch

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-012 Route of Administration TOPICAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 400 mg

  Inactive Ingredients Ingredient Name Strength ACRYLIC ACID (UNII: J94PBK7X8S)   ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)   CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)   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)

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-012-05 1 in 1 CARTON 1 5 in 1 POUCH

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/12/2011

  Labeler - CHAIN DRUG MARKETING ASSOCIATION INC (011920774)

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