Label: DICLOFENAC SODIUM TOPICAL GEL, 1% (diclofenac sodium topical gel, 1%- nsaid gel

  • NDC Code(s): 73715-005-01
  • Packager: Mohnark Pharmaceuticals Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated January 10, 2023

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

  • ACTIVE INGREDIENT

    Diclofenac sodium (NSAID*) 1%
    *nonsteroidal anti‑inflammatory drug

  • INACTIVE INGREDIENTS

    Inactive ingredients:

    Carbomer Homopolymer Type C, Coco-Caprylate/caprate, Isopropyl Alcohol, Mineral Oil, Polyoxyl 20 Cetostearyl Ether, Propylene Glycol, Purified Water, Strong Ammonia Solution

  • PURPOSE

    Arthritis pain reliever

  • USES

    for the temporary relief of arthritis pain ONLY in the following areas:

    • hand, wrist, elbow (upper body areas)
    • foot, ankle, knee (lower body areas)

    this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use

  • WARNINGS

    For external use only

    Allergy alert: Diclofenac may cause a severe allergic reaction, especially in people allergic to aspirin.

    Symptoms may include:

    • hives • asthma (wheezing) • skin reddening • blisters • facial swelling • shock • rash

    If an allergic reaction occurs, stop use and seek medical help right away.

    Liver warning: This product contains diclofenac. Liver damage may occur if you apply

    • more or for a longer time than directed
    • when using other drugs containing diclofenac

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

    • are age 60 or older
    • have had stomach ulcers or bleeding problems
    • take a blood thinning (anticoagulant) or steroid drug
    • take other drugs containing prescription or non-prescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
    • have 3 or more alcoholic drinks every day while using this product
    • apply more or for longer than directed

    Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

  • DO NOT USE

    • if you have ever had an allergic reaction to any other pain reliever or to a fever reducer
    • for strains, sprains, bruises or sports injuries. This product has not been shown to work for these types of injuries.
    • right before or after heart surgery
    • on more than 2 body areas at the same time
    • in the eyes, nose or mouth
  • ASK A DOCTOR BEFORE USE IF

    • you have problems or serious side effects from taking pain relievers or fever reducers
    • stomach bleeding warning applies to you you have a history of stomach problems, such as heartburn
    • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
    • you are taking a diuretic
    • you are under age 18 years. It is not known if this drug works or is safe in children under age 18 years.
  • ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

    • under a doctor’s care for any serious condition
    • taking any other drug
  • WHEN USING THIS PRODUCT

    • avoid contact with eyes, nose, or mouth
    • if eye contact occurs, rinse thoroughly with water
  • STOP USE AND ASK A DOCTOR IF

    • pain gets worse or lasts more than 21 days
    • redness or swelling is present in the painful area
    • fever occurs
    • skin irritation occurs
    • any new symptoms appear. These could be signs of a serious condition.
    • you experience any of the following signs of stomach bleeding
    • feel faint
    • have bloody or black stools
    • vomit blood
    • have stomach pain that does not get better
    • you have symptoms of heart problems or stroke
    • chest pain
    • trouble breathing
    • leg swelling
    • weakness in one part or side of body
    • slurred speech
  • IF PREGNANT OR BREAST-FEEDING

    ask a health professional before use. It is especially important not to use this product during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    Use up to 21 days unless directed by your doctor

    Not for strains, sprains, bruises or sports injuries. This product has not been shown to work for these types of injuries.

    For your arthritis pain:Daily Per Dose

    Use 4 times per day every day
    Do not use on more than 2 body

    areas at the same time

    Use DOSING GUIDE to measure a dose

    For each upper body area (hand, wrist, or elbow)

    - Squeeze out 2.25 inches (2 grams)

    For each lower body area (foor, ankle or knee) -

    Squeeze out 4.5 inches (4 grams)

    Read the entire directions on carton for instructions:

    use only as directed
    do not use more than directed or for longer than directed
    apply only to clean, dry skin that does not have any cuts, open wounds, infections or rashes
    do not apply in same area as any other product
    do not apply with external heat such as heating pad
    do not apply a bandage over the treated area

    store Diclofenac Sodium Gel with carton and dosing guide as shown.

  • OTHER INFORMATION

    • Store at 20-25°C (68°F - 77°F). Keep from freezing.
    • read all product information before using. Keep from freezing. read all product information before using. Keep this carton for important information.

    Inactive ingredients

    Carbomer homopolymer Type C, cocoyl caprylocaprate, ispropyl alcohol, mineral oil, polyoxyl 20 cetostearyl ether, propylene glycol, purified water, strong ammonia solution.

    Question and comments: 1-866-611-5206

  • INDICATIONS AND USAGE

    Diclofenac is a nonsteroidal anti-inflammatory drug (NSAID). This medicine works by reducing substances in the body that cause pain and inflammation.

    Diclofenac is used to treat mild to moderate pain, or signs and symptoms of osteoarthritis or rheumatoid arthritis.

  • PRINCIPAL DISPLAY PANEL

    Carton Label - NDC 73715-005-01

    Diclofenac Sodium Topical Gel, 1%

    (NSAID)- Arthritis pain reliever

    For external use only

    For daily Treatment of Arthritis Pain Anti-Inflammatory

    Net Wt 1.76 oz (50g)

    Container Label

  • INGREDIENTS AND APPEARANCE
    DICLOFENAC SODIUM TOPICAL GEL, 1% 
    diclofenac sodium topical gel, 1% (nsaid) gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73715-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DICLOFENAC SODIUM (UNII: QTG126297Q) (DICLOFENAC - UNII:144O8QL0L1) DICLOFENAC SODIUM1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIA (UNII: 5138Q19F1X)  
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73715-005-0150 g in 1 CARTON; Type 0: Not a Combination Product08/31/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21098608/31/2021
    Labeler - Mohnark Pharmaceuticals Inc. (117013830)
    Registrant - Mohnark Pharmaceuticals Inc. (117013830)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mohnark Pharmaceuticals Inc117013830manufacture(73715-005)