PAINPATROL CBD PROFESSIONAL PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) GEL [SMARTSCIENCE LABORATORIES, INC.]

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  • PAINPATROL CBD PROFESSIONAL PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) GEL [SMARTSCIENCE LABORATORIES, INC.]

PAINPATROL CBD PROFESSIONAL PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) GEL [SMARTSCIENCE LABORATORIES, INC.]
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NDC 64479-201-11
Set ID ecc8f4c5-2ccb-4d54-a3c1-b9b8d0ad8a50
Category HUMAN OTC DRUG LABEL
Packager SmartScience Laboratories, Inc.
Generic Name
Product Class
Product Number
Application Number PART348
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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Natural Menthol, USP (8.5%)

  • Purpose

    Topical Analgesic

  • Uses

    Temporarily relieves foot, ankle and leg pain associated with:

    • arthritis
    • muscle aches
    • muscle strains
    • muscle sprains
    • joint pain
  • Warnings

    For external use only: Flammable: Keep away from excessive heat or open flame.

    • Ask a doctor before use is you have sensitive skin or if you are taking any blood thinners,

    When using this product

    Do not use on wounds or irritated skin

    • Do not bandage tightly or usewith a heating pad
    • Wash hands after use with cool water

    • If pregnant or breast feeding, ask a health professional before use

    • Keep out of reach of children. If accidentally swallowed,contact a doctor or poison control center immediately

    • Stop use and ask a doctor if condition worsens or if pain persists for more than 7 days, or clears up, then reoccurs within a few days.
  • Directions

    Use only as directed

    • Do not use on children under 12 years of age.
    • Roll onto affected area no more than four times daily. Shake well before each use.
  • Inactive Ingredients

    Aloe Barbadensis Leaf Extract, Arnica Montana Extract, Boswellia Serrata Extract, Camphor, Cannabis Sativa Seed Oil (Hemp Derived), Carbomer, Chondroitin Sulfate, Glucosamine Sulfate, Glycerin, Ilex Paraguarensis Extract, Isopropyl Alcohol, Methyl Paraben, Methylsulfonylmethane, Peppermint Oil, Polysorbate 20, Propylene Glycol, Purified Water,Triethanolamine.

  • Other Information

    Questions or comments?

    Call (877) 383-2334.

    Store in a cool dry place with the cap tightly closed. Note: Because this product contains natural ingredients, color may vary.

  • SPL UNCLASSIFIED SECTION

    Manufactured by: SmartScience Laboratories, Inc.
    13760 Reptron Blvd., Tampa, FL 33626

  • PRINCIPAL DISPLAY PANEL - 88 ML Bottle Label

    Clinical Strength Menthol Formula

    PainPatrol™
    CBD
    Professional Pain Relief

    Pain Relief for arthritis, joints and muscles
    Also contains Glucosamine • Chondroitin • Arnica • Boswellia

    150mg CDB
    No Mess Applicator.
    3FL OZ (88ML)

    Principal Display Panel - 88 ML Bottle Label
  • INGREDIENTS AND APPEARANCE
    PAINPATROL CBD PROFESSIONAL PAIN RELIEF 
    menthol, unspecified form gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64479-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM85 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARNICA MONTANA (UNII: O80TY208ZW)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64479-201-1188 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product04/20/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34804/20/2019
    Labeler - SmartScience Laboratories, Inc. (035907919)
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