Label: DICLOFENAC SODIUM- diclofenac sodium 1% gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated October 12, 2023

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

  • ACTIVE INGREDIENT

    (NSAID) - arthritis pain reliever

    Active ingredient

    Diclofenac sodium (NSAID*) 1%

    *nonsterodial anti-inflammatory drug

  • PURPOSE

    Purpose

    Arthritis pain reliever

  • INDICATIONS & USAGE

    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 not pain relief in 7 days, stop use

  • WARNINGS

    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 contain an NSAID, which may cause severe stomach bleeding. The chance is small but high 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 attach, heart failure, and stroke. These can be fatal. The rish is higher if you use more than directed or for longer than directed.

  • DO NOT USE

    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 DOCTOR

    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 or you have a history of stomach prohlems, 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 the age of 18 years. It is not known if this drug works or is safe in children under age 18 years.
  • ASK DOCTOR/PHARMACIST

    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

    When using this product

    • avoid contact with eyes, nose, or mouth
    • if eye contact occurs, rinse thoroughly with water
  • STOP USE

    Stop use and ask a doctor if

    • pain gets worse or last 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 heat problems or stroke
    • chest pain
    • trouble breathing
    • leg swelling
    • weakness in one part or side of body
    • slurred speech
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding

    ask a health care 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

    Keep our of reach of children

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

  • DOSAGE & ADMINISTRATION

    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.

    Daily For arthritis pain:

    Use 4 times per day every day
    Do not use on more than 2 body areas at the same time

    • Per Dose (Use ENCLOSED DOSING CARD 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 (foot, ankle, or knee) - Squeeze out 4.5 inches (4 grams)

    Read the enclosed User Guide for complete 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 the 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 ENCLOSED DOSING CARD with your Diclofenac Sodium Topical Gel, 1% Arthritis Pain. The dosing card is re-usable.

  • OTHER SAFETY INFORMATION

    Other Information

    • Store at 20-25°C (68°F - 77°F). Keep from freezing.
    • read all product information before using. Keep the dossing card, the carton and accomanying User guide for important information.
  • INACTIVE INGREDIENT

    Inactive ingredients

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

  • QUESTIONS

    Questions and comments 1-866-747-7365

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

    Carton Label - 100g

    NDC 70512-106-10

    ORIGINAL PRESCRIPTION STRENGTH

    Diclofenac Sodium Topical Gel, 1%

    (NSAID)- Arthritis pain reliever

    For daily Treatment of Arthritis Pain Anti-Inflammatory

    For external use only

    Net Wt. 3.53 oz (100 g)

    Diclofenac Carton

    Tube Label- 100g

    NDC 70512-106-10

    Diclofenac Sodium Topical Gel, 1%

    (NSAID)- Arthritis pain reliever

    For external use only

    Net Wt 3.53 oz (100 g)

    Diclofenac Tube

  • INGREDIENTS AND APPEARANCE
    DICLOFENAC SODIUM 
    diclofenac sodium 1% gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70512-106
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DICLOFENAC SODIUM (UNII: QTG126297Q) (DICLOFENAC - UNII:144O8QL0L1) DICLOFENAC SODIUM10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMMONIA (UNII: 5138Q19F1X)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70512-106-101 in 1 CARTON03/17/2021
    1100 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21098603/17/2021
    Labeler - SOLA Pharmaceuticals (080121345)