Label: GOLD ICE PAIN RELIEF- menthol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active Ingredient

    Menthol 6.25%

    Purpose

    External Analgesic

  • Uses

    temporary relief of minor aches and pains of muscles and joints associated with: 

    • simple backache 
    • arthritis
    • strains
    • bruises
    • sprains
  • Warnings:

    For external use only

    Keep away from fire or flame Flammable:

    When using this product

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

    Stop Use and ask a Doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clears up and occur again within a few days.
    • redness or skin irritation occurs

    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

    apply to affected area not more than 3 to 4 times daily Adult and children 12 years of age and over:

    consult a physician Children under 12 years of age:

  • Other information

    • close container tightly and store at room temperature 
    • do not use if plastic seal around cap is broken or missing
    • store in a cool, dry place
  • Inactive Ingrediets

    Beeswax, Capsicum Frutescens Fruit Powder, Lavandula Angustifolia (Lavender) Flower Extract, Lavandulaangustifolia (lavender) Oil, Mentha Piperita (Peppermint) Leaf, Rosmarinus officinalis (Rosemary) Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Oil, Verbascum Thapsus Extract

  • Questions or Comments?

    Sprigs Life Inc PO Box 387 

    Millersburg, Ohio 44654 1-888-990-7763

    Mon-Fri 8am-3pm EST

  • Package Labeling:

    Label4Label5

  • INGREDIENTS AND APPEARANCE
    GOLD ICE PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72226-305
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL62.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    TABASCO PEPPER (UNII: J1M3NA843L)  
    LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    MENTHA PIPERITA LEAF (UNII: A389O33LX6)  
    ROSEMARY (UNII: IJ67X351P9)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72226-305-001 in 1 BOX08/01/2020
    1100 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/01/2020
    Labeler - Eden's Answers, Inc. (030063091)
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