Label: MINERAL ICE QUICK DRY FOAM- menthol aerosol, foam

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

Drug Label Information

Updated December 15, 2023

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  • Active Ingredient

    Menthol 10%

  • Purpose

    Topical analgesic

  • Uses

    ● temporarily relieves minor aches and pains of muscles and joints associated with:

    ● arthritis ● simple backache ● strains

    ● bruises ● sprains

    ● provides cooling penetrating relief

  • Warnings

    For external use only

    Contents under pressure. Do not puncture or incinerate. Avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes.

    Do not use

    ● with other topical pain relievers

    ● with heating pads or heating devices

    When using this product

    ● do not use in or near the eyes

    ● do not apply to wounds or damaged skin

    ● do not bandage tightly

    Stop use and ask a doctor if

    • condition worsens

    • symptoms last 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.

  • Directions

    ● clean affected area before applying product ● hold can at an angle and press nozzle lightly ● dispense onto hand and then apply to target area ● wipe nozzle clean after each use ● replace the overcap after each use ● adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily ● children under 2 years of age: ask a doctor

  • Other Information

    ● store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature] ● do not store at temperatures above 50°C

  • Inactive ingredients

    Aluminum Starch Octenylsuccinate, Caprylyl Glycol, Cetyl Alcohol, Cocamidopropyl Betaine, Ethanol, Isobutane, Phenoxyethanol, Purified Water, Sodium Chloride, Vinyl Caprolactam/VP/Dimethylaminoethyl Methacrylate Copolymer

  • Questions?

    Call 1-833-279-6522

  • Additional Information Listed on Other Panels

    ©2020 Crown Laboratories, Inc.

    Distributed by: Crown Laboratories, Inc.

    Johnson City, TN 37604 Made in USA

    P11842.00 DOT 2Q M5706

  • Mineral Ice Quick Dry Foam - 4 oz Canister Label

    NDC 0316-0290-04

    NEW

    ORIGINAL THERAPEUTIC

    Mineral Ice QUICK DRY FOAM

    MENTHOL PAIN RELIEVING FOAM

    MAXIMUM STRENGTH

    Greaseless with DEEPCOLD Pain Reliever

    Net wt. 4 oz (113 g)

    mineralicefoam

  • INGREDIENTS AND APPEARANCE
    MINERAL ICE QUICK DRY FOAM 
    menthol aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0290
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    2-(DIBUTYLAMINO)ETHYL METHACRYLATE (UNII: XE2SIC67YA)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    ISOBUTANE (UNII: BXR49TP611)  
    WATER (UNII: 059QF0KO0R)  
    N-VINYLCAPROLACTAM (UNII: KFC10CY9UP)  
    N-VINYLPYRROLIDINONE (UNII: 76H9G81541)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0316-0290-04113 g in 1 CANISTER; Type 0: Not a Combination Product04/30/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/30/202107/31/2024
    Labeler - Crown Laboratories (079035945)
    Registrant - Crown Laboratories (079035945)
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