Label: VIVA PATCH- camphor, lidocaine, and methyl salicylate patch

  • NDC Code(s): 53225-1030-1, 53225-1030-2
  • Packager: Terrain Pharmaceuticals
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • DRUG FACTS

    DRUG FACTS

  • Active Ingredient

    Camphor 2%

  • Purpose

    Topical Analgesic

  • Active Ingredient

    Lidocaine 2.5%

  • Purpose

    Topical Anesthetic

  • Active Ingredient

    Methyl Salicylate 4%

    (NSAID: nonsteroidal anti-inflammatory drug)

  • Purpose

    Topical Analgesic

  • Uses

    Temporarily relieves mild to moderate aches and pains of muscles and joints associated with:

    • muscle soreness

    • strains

    • sprains

    • arthritis

    • simple backache

    • muscle stiffness

    • bruises

  • Warnings

    For external use only

    Stomach bleeding warning

    This product contains an NSAID, which may cause stomach bleeding. The chance is small, but higher if you

    • are age 60 or older

    • have had stomach ulcers or bleeding problems

    • take other drugs containing an NSAID (Aspirin, Ibuprofen, Naproxen, or others)

    • take a blood thinning (anticoagulant) or steroid drug

    • have three or more alcoholic drinks every day while using this product

    • take more or for a longer time than directed

    Do not use

    • on the face or rashes; on wounds or damaged skin

    • in the eyes, mouth, or other mucous membranes

    • on genitals

    • with a heating pad

    • if allergic to any NSAIDS

    • right before or after heart surgery

    • any patch from a pouch that has been opened for 7 or more days

    Ask a doctor before use if

    • you are allergic to topical products

    • the stomach bleeding warning applies to you

    • you are taking a diuretic

    • you have high blood pressure, heart disease, or kidney disease

    • you are pregnant

    When using this product

    • wash hands after applying or removing patch

    • avoid contact with eyes. If eye contact occurs, rinse thoroughly with water

    • the risk of heart attack or stroke may increase if you use more than directed or for longer than directed.

    Stop use and consult your physician if

    • stomach pain or upset gets worse or lasts

    • rash, irritation, or itching develops

    • you feel faint, vomit blood, or have bloody or black stools (these are signs of stomach bleeding)

    • condition worsens

    If pregnant or breast feeding,

    ask a doctor before use while breast feeding and during the first 6 months of pregnancy. Do not use during last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery.

    Keep out of reach of children.

    If put in mouth, get medical help or contact a Poison Control Center right away. Package not child resistant. Dispose of the used patches by folding sticky ends together.

  • Directions

    Adults, or children over the age of 12:

    • Apply patch to affected area 1 to 2 times daily or as directed.

  • Instructions for Use

    • clean and dry affected area

    • open pouch and remove one patch

    • remove protective film from patch

    • apply one patch to the affected area of pain and leave in place for 8 to 12 hours

    • if pain lasts after using the first patch, a second patch may be applied for up to another 8 to 12 hours

    • only use one patch at a time

    • do not use more than 2 patches per day

    • wash hands with soap and water after applying or removing patch

    • reseal pouch containing unused patches immediately after each use

    Children under 12 years of age: Do not use

  • Other Information

    • some individuals may not experience pain relief until several minutes or hours after applying the patch

    • store in a cool, dry place

    • protect product from excessive moisture or sunlight

    • store at 67-77°F (19-25°C)

  • INACTIVE INGREDIENT

    Acrylic Acid, Aluminum Hydroxide, Carmellose Sodium, 2-Ethylhexyl Acrylate, Glycerin, Isopropyl Myristate, Methyl Acrylate, Nonoxynol-30, Polyacrylic Acid, Polysorbate 80, Sodium Polyacrylate, Sorbitan Sesquioleate, Starch, Talc, Tartaric Acid, Titanium Dioxide, Water

  • SPL UNCLASSIFIED SECTION

    Terrain Pharmaceuticals

    Reno, NV 89501

    TerrainRx.com

    877-985-8377

    Get Back to Life TM

    VIVAPatch.com

    Engineered in Reno-Tahoe

    Assembled in China

    Lot Number:

    Exp Date:

  • Principal Display Panel

    VIVAPatch-Box

    NDC 53225-1030-1

    VIVA PATCH

    SOOTHING PAIN RELIEF

    LIDOCAINE - METHYL SALICYATE - CAMPHOR

    • Reduced Scent
    • Flexible & Form Fitting
    • Deep Penetrating
    • Fast Acting

    GET BACK TO LIFE TM

    15 Patches

  • INGREDIENTS AND APPEARANCE
    VIVA PATCH 
    camphor, lidocaine, and methyl salicylate patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53225-1030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE2.5 mg  in 100 mg
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)2 mg  in 100 mg
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE4 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    NONOXYNOL-30 (UNII: JJX07DG188)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL ACRYLATE (UNII: WC487PR91H)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53225-1030-15 in 1 BOX08/31/2016
    13 in 1 POUCH
    18650 mg in 1 PATCH; Type 0: Not a Combination Product
    2NDC:53225-1030-21 in 1 BOX08/31/201612/16/2019
    23 in 1 POUCH
    28650 mg in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/31/2016
    Labeler - Terrain Pharmaceuticals (078358750)
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