LifeSource Vitamins
Rated 4.83 out of 5
6 Reviews

Shark Cartilage 750 mg - 100 Capsules

Original Price: $16.99   Current Price: $16.99
  • Supports joint comfort and mobility*
  • Supports healthy connective tissue*
  • Supports cartilage health and function*
  • Supports natural inflammatory response*
  • Supports immune function and wellness*
  • Supports skin hydration and elasticity*
  • High-potency 2,250 mg shark cartilage*
  • Third-Party Tested for Purity & Quality*
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Product Details

LifeSource Vitamins Shark Cartilage 750 mg β€” Capsules, 100 Count β€” Supports Joint & Immune Health*

Pure, freeze-dried shark cartilage supplying naturally occurring chondroitin sulfates & glycosaminoglycans (GAGs) to support joint comfort, everyday mobility, and immune balance. Produced in FDA-registered, GMP-certified facilities and 3rd-party tested for identity, potency & purity.*

Research-Driven & Verified Product.
Explore the clinical research, ingredient science, and global evidence supporting this product below.
Research Promise: At LifeSource Vitamins, our commitment is rooted in research and results. Every benefit below is supported by human clinical studies indexed in the National Institutes of Health (NIH) via PubMed, with full texts available in the National Library of Medicine (NLM) PubMed Central (PMC) when available. In addition, we reference reviews from 39 leading health organizations and insights from 20 top global universities to ensure our guidance aligns with credible science.*
Clinically Studied Benefits

βœ“ Supports joint comfort in osteoarthritis β€” Chondroitin sulfate modestly improves pain and function vs placebo in human trials and meta-analyses. NIH/PubMed β€” Singh, 2015

βœ“ Helps daily mobility β€” Chondroitin sulfate recommended within multimodal care for osteoarthritis symptoms. NIH/PMC β€” Henrotin, 2010

βœ“ Joint symptom support β€” Fixed-dose glucosamine + chondroitin regimens non-inferior to reference products in knee OA RCTs. NIH/PubMed β€” Lomonte, 2021

βœ“ OA pain/function short-term benefit β€” Meta-analysis shows small but meaningful average improvements with chondroitin. NIH/PubMed β€” Singh, 2015

βœ“ Supports cartilage matrix integrity (context) β€” Chondroitin contributes to structure-functional role in cartilage. NIH/PMC β€” Henrotin, 2010

βœ“ Anti-angiogenic activity in dermatologic context β€” Shark cartilage extract demonstrated effects with potential relevance (non-OA). NIH/PubMed β€” Dupont, 1998

βœ“ Angiogenesis pathway modulation (clinical context) β€” Cartilage-derived extract studied for anti-angiogenic effects. NIH/PubMed β€” Gingras, 2001

βœ“ Supports balanced inflammatory response (context) β€” GAGs and cartilage extracts explored in inflammatory models. NIH/PMC β€” Chen, 2012

βœ“ OA symptom improvement in combinations β€” Glucosamine + chondroitin shows benefits in subsets of patients. NIH/PubMed β€” Lomonte, 2021

βœ“ General tolerability in clinical use β€” Well-tolerated with noted cautions (e.g., calcium content). NIH/PubMed β€” Singh, 2015

Additional / Promising Evidence

βœ“ Cartilage constituents & immune balance β€” Preclinical/adjunct literature on GAGs in inflammatory models. NIH/PMC β€” Chen, 2012

βœ“ Mechanistic OA support β€” Structure-functional rationale for chondroitin in cartilage matrix. NIH/PMC β€” Henrotin, 2010

βœ“ OA symptom improvement (combinations) β€” Trials show symptomatic benefits in subsets. NIH/PubMed β€” Lomonte, 2021

βœ“ Dermatology context β€” Anti-angiogenic properties referenced in psoriasis literature. NIH/PubMed β€” Dupont, 1998

βœ“ Angiogenesis pathway research β€” Cartilage-derived extract in oncology context studies. NIH/PubMed β€” Gingras, 2001

βœ“ Evidence limitations noted β€” Mixed/insufficient data for many uses; safety emphasized. NIH/PubMed β€” Singh, 2015

University-Led & Academic Studies

βœ“ University-affiliated rheumatology centers β€” Meta-analyses and RCTs on chondroitin sulfate for OA. NIH/PubMed β€” Singh, 2015

βœ“ European university laboratories β€” Mechanistic reviews on chondroitin’s role in cartilage. NIH/PMC β€” Henrotin, 2010

βœ“ Canadian academic oncology groups β€” Clinical studies on cartilage-derived anti-angiogenic extract. NIH/PubMed β€” Batist, 2002

We monitor research from leading institutions β€” Harvard, Johns Hopkins, Mayo Clinic, Cleveland Clinic, Cambridge, Oxford, Stanford, Yale, Tufts, University of Florida, Oregon State University – Linus Pauling Institute, Columbia, Cornell, Ohio State β€” to align with credible science.*
Key Ingredients
  • Shark Cartilage Powder β€” Natural source of chondroitin sulfates & GAGs that help support joint comfort and cartilage matrix integrity.*
Brief Benefit Bullets
  • Helps support joint comfort & daily mobility (chondroitin-rich)*
  • Supplies GAGs that help nourish cartilage matrix (structure & lubrication)*
  • Supports balanced inflammatory response (evidence mixed; see studies)*
  • Historical use in dermatology/immune contexts (see research notes)*
  • 3rd-party lab tested for identity, potency & purity
Suggested Use

Take 3 capsules daily with meals, or as directed by your healthcare professional. Do not use if allergic to fish. If pregnant, nursing, taking medications, or have a medical condition, consult your physician.*

Product Specifications

β€’ Serving Size β€” 3 capsules (2,250 mg shark cartilage)

β€’ Per Capsule β€” 750 mg shark cartilage (100 capsules per bottle)

β€’ Other Ingredients β€” Gelatin (bovine) capsules

β€’ Allergen Note β€” Contains finfish (per label)*

β€’ Quality β€” Third-party tested for identity, potency & purity

3rd-Party Testing: Every batch is independently verified for identity, potency, and purity.
Click here to see our 3rd-party testing.

LifeSource Vitamins β€” Proudly American β€” Since 1992

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

Shark Cartilage 750 mg β€” natural chondroitin & GAGs for joint comfort and mobility. 3-caps serving = 2,250 mg. 3rd-party tested. Clinically Studied Ingredients β€” NIH/PubMed!*

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