Label: LINIMENT- menthol gel

  • NDC Code(s): 70489-1811-1, 70489-1811-2
  • Packager: INNOVACYN INC.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 5, 2023

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

  • Active Ingredient

    MENTHOL

  • Description

    Vetericyn Mobility Liniment is formulated with fast-acting ingredients to

    refresh tired and worked muscles. It melts on contact and works quickly

    to reduce swelling and pain of sore muscles and joints, helping to relieve

    stiffness and soreness caused by strenuous activity.

  • Dosage/Administration

    Directions for Use: Apply Vetericyn Liniment and gently massage into the

    affected area for relief of muscular and joint soreness, swelling, and stiffness. For deeper

    penetrating relief, apply under wraps and  bandages.

  • General Precautions

    Use Precautions: Use only as directed.

    For external use only.

    Discontinue use if skin irritation develops and contact your veterinarian. For animal use only, not for human use.

    Keep out of reach of children.

    For horses not intended for human consumption.

  • Questions

    vetericyn.com | 866.318.3116 

  • SPL UNCLASSIFIED SECTION

  •  Precautions

    Storage: Store at room temperature away from direct sunlight and heat. If accidentally frozen,

    shake contents before use. Do not use after expiration date. After use, seal or close dispenser.

    Disposal: No special disposal requirements.

    Stability: See expiration date on bottom of bottle.

  • Inactive Ingredient

    Purified

    Water, Ethyl Alcohol, Isocetyl Stearate, Glycerine,

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer,

    Bisabolol, Heterotheca Inuloides Flower Extract

    (and) Glycerin, Tocopherol (Vitamin E), Dimethicone,

    Mentha Piperita (Peppermint) Oil, Helianthus Annuus

    (Sunflower) Seed Oil, Phenoxyethanol, Triethanolamine,

    Propylene Glycol / Menthol / Methyl Diisopropyl

    Propionamide / Ethyl Menthane Carboxamide /

    Methyl Lactate / Hydroxypropylcellulose / Acrylates,Copolymer, FD&C Blue #1

  • Product label

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    LINIMENT 
    menthol gel
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:70489-1811
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL7 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ISOCETYL STEARATE (UNII: 3RJ7186O9W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    HETEROTHECA INULOIDES FLOWER (UNII: W9NZ9OZF68)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SUNFLOWER SEED (UNII: R9N3379M4Z)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)  
    ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)  
    METHYL LACTATE, (-)- (UNII: 0379G9C44S)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70489-1811-189 mL in 1 BOTTLE
    2NDC:70489-1811-2473 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/01/2021
    Labeler - INNOVACYN INC. (025217003)