Label: CBD PAIN RELIEF ROLL ON- menthol, unspecified form gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 10, 2020

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Natural Menthol, USP (8.5%)

  • Purpose

    Topical Analgesic

  • Uses

    Temporary relief from minor aches and pains from sore muscles and joints, backache, arthritis.

  • Warnings

    For external use only. Flammable.

    Keep out of reach of children.

    Contact a doctor before using if have sensitive skin or are pregnant, breastfeeding or on any medications. If swallowed get medical help or call Poison control center immediately.

    When using this product

    Do not use with heating pad. Do not bandage. Wash hands with cold water immediately after use and do not touch eyes or mucous membranes. Stop use and ask a doctor if redness or irritation occurs, if condition worsens, or if pain persists for more than 7 days or clears up, then reoccurs.

  • Directions

    Use only as directed. Shake well before each use. Roll-on to affected area no more than four times daily. Do not use on children under 12 years of age.

  • 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 Paraguariensis Extract, Isopropyl Alcohol, Methyl Paraben, Methylsulfonylmethane, Peppermint Oil, Polysorbate 20, Propylene Glycol, Purified Water, Triethanolamine.

  • Other Information

    Email Questions: info@invigcbd.com. Store in a cool dry place with the cap tightly closed. Note: Because this product contains natural ingredients, colors may vary. NDC 64479-401-01

  • SPL UNCLASSIFIED SECTION

    Manufactured cGMP by
    Smart Science Labs,
    13760 Reptron Blvd Tampa, FL. 33626

  • PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

    INVIG

    CBD
    Pain Relief
    Roll On

    • Thc Free
    • Fast-acting relief
    • Broad-Spectrum
      Hemp CBD

    www.invigcbd.com

    150 mg CBD
    3 fl oz (88ml)

    PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label
  • INGREDIENTS AND APPEARANCE
    CBD PAIN RELIEF ROLL ON 
    menthol, unspecified form gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64479-401
    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 POTASSIUM CHLORIDE (UNII: 15VQ11I66N)  
    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:64479-401-0188 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product02/12/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34802/12/2020
    Labeler - SmartScience Laboratories, Inc. (035907919)