Label: DURAFLEX- ascorbic acid, calcium, glucosamine sulfate, chondroitin sulfate, msm and cat claw. tablet

  • NHRIC Code(s): 43063-965-60, 43063-965-98
  • Packager: PD-Rx Pharmaceuticals, Inc.
  • Category: DIETARY SUPPLEMENT
  • DEA Schedule: None
  • Marketing Status: Dietary Supplement

Drug Label Information

Updated July 16, 2021

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

  • HEALTH CLAIM:

    DURAFLEX TABLETS - Dietary Supplement     

    image description

    OTHER INGREDIENTS:  cellulose, stearic acid, silicon dioxide, croscamellose sodium, magnesium stearate, ethycellose.

  • DESCRIPTION:

    duraflex is formulated to help support healthy, mobile joint function and connective tissue, and therefore, support the comfortable freedom of movement often lost as we age. When taken daily over time, duraflex helps protect cartilage from occasional overexertion and physical activity as it provides the nourishment your body needs to support cartilage, lubricate, and strengthen your joints. duraflex has key dietary ingredients, including: Glucosamine; Chondroitin; Methylsulfonylmethane (MSM). With daily use, benefits may be felt in as little as four weels.

    The above statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

  • WARNING AND PRECAUTIONS

    Pregnant or lactating women should consult a doctor using any product. Avoid product if you have allergies to shellfish. Consult doctor before use if you have, or have had, thyroid or prostate disorders, diabetes, hypoglycemia, asthma, or if you are on a sodium restricted diet or if you are taking ANY MEDICATIONS OR REMEDIES such as blood thinners or daily aspirin. Discontinue use and consult your doctor before use if any adverse reactions occur, such as gastointestinal discomfort, allergic reaction, any skin irritation, fatigue, dizziness, pain, hair loss, irregular heartbeat, or changes in blood pressure or mood. NOT INTENDED FOR USE BY PERSONS UNDER THE AGE OF 18.

    WARNING: If you are pregnant, nursing a baby, recovering from recent surgery or have a heart or circulatory condition, consult a physician before using this product.

  • ADVERSE REACTIONS

    ALLERGEN WARNING: CONTAINS SHELLFISH

  • DOSAGE & ADMINISTRATION

    duraflex tablet dosage- Take 4 tablets daily for 1-2 months, then reduce dosage to a minimum of 2 tablets daily to maintain comfortable movement


  • HOW SUPPLIED HEALTH CLAIM:

    duraflex Dietary Supplement
    tablets are brown
    Bottles of 60 tablets NDC 43063-965-60
    Bottles of 120 tablets NDC 43063-965-98

    duraflex is a registered trademark of PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 405-942-3040

  • STORAGE AND HANDLING:

    Tamper-Evident Feature- This bottle is sealed with a tamperevident safety seal for your protection. Do not use if this seal is missing or broken.

  • PACKAGE LABEL:

    43063965 Label

  • INGREDIENTS AND APPEARANCE
    DURAFLEX 
    ascorbic acid, calcium, glucosamine sulfate, chondroitin sulfate, msm and cat claw. tablet
    Product Information
    Product TypeDIETARY SUPPLEMENTItem Code (Source)NHRIC:43063-965
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID60 mg
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) (CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS - UNII:L11K75P92J) DIBASIC CALCIUM PHOSPHATE DIHYDRATE49 mg
    CHONDROITIN SULFATE SODIUM (BOVINE) (UNII: 8QTV3DTT8W) (CHONDROITIN SULFATE (BOVINE) - UNII:6IC1M3OG5Z) CHONDROITIN SULFATE (BOVINE)150 mg
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H) (DIMETHYL SULFOXIDE - UNII:YOW8V9698H) DIMETHYL SULFOXIDE125 mg
    CAT'S CLAW (UNII: 9060PRM18Q) (CAT'S CLAW - UNII:9060PRM18Q) CAT'S CLAW175 mg
    Inactive Ingredients
    Ingredient NameStrength
    GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N) 375 mg
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NHRIC:43063-965-6060 in 1 BOTTLE, PLASTIC
    2NHRIC:43063-965-98120 in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    dietary supplement07/16/2021
    Supplement Facts
    Serving Size : Serving per Container :
    Amount Per Serving% Daily Value
    color
    scoring1
    size (solid drugs)21 mm
    shape
    Labeler - PD-Rx Pharmaceuticals, Inc. (156893695)
    Registrant - PD-Rx Pharmaceuticals, Inc. (156893695)
    Establishment
    NameAddressID/FEIBusiness Operations
    PD-Rx Pharmaceuticals, Inc.156893695repack(43063-965)