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

duraflex by

Drug Labeling and Warnings

duraflex by is a Other medication manufactured, distributed, or labeled by PD-Rx Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HEALTH CLAIM:

DURAFLEX TABLETS - Dietary Supplement     

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:

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	DIETARY SUPPLEMENT	Item Code (Source)	NHRIC:43063-965
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	60 mg
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) (CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS - UNII:L11K75P92J)	DIBASIC CALCIUM PHOSPHATE DIHYDRATE	49 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 SULFOXIDE	125 mg
CAT'S CLAW (UNII: 9060PRM18Q) (CAT'S CLAW - UNII:9060PRM18Q)	CAT'S CLAW	175 mg

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NHRIC:43063-965-60	60 in 1 BOTTLE, PLASTIC
2	NHRIC:43063-965-98	120 in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
dietary supplement		07/16/2021

Supplement Facts
Serving Size :		Serving per Container :
	Amount Per Serving	% Daily Value
color
scoring	1
size (solid drugs)	21 mm
shape

Labeler - PD-Rx Pharmaceuticals, Inc. (156893695)

Registrant - PD-Rx Pharmaceuticals, Inc. (156893695)

Establishment
Name	Address	ID/FEI	Business Operations
PD-Rx Pharmaceuticals, Inc.		156893695	repack(43063-965)