Black Seed Oil - Ancient Remedy
Healing Properties Known for Thousands of Years
Now Backed by Modern Science
DISCOVER THE TRUTH!

What is black seed oil and what secrets does it hold for health and wellness?

Black seed oil (BSO) comes from the black cumin seed (Nigella sativa). It has been use for millennia in many different forms. In order to understand what it is and the potential it holds, we will look at the following 11 areas. We will use the most current research to shed light on each of these subjects. There will be a link at the bottom of this page to an in-depth article with over 240 sources.
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  • Ancient Origins: the history of black seed oil
  • Nutrient Dense: the chemical properties of black seed oil and the nutrients it provides
  • Versatile: the history of its use
  • ​Anti-inflammatory: the properties that allow BSO to help with pain and inflammation
  • ​Microbial Defense: the immunity enhancing capabilities of BSO
  • ​Heart Health: the cardiovascular properties of BSO 
  • ​Brain Health: the neurological potential of BSO
  • ​Gut Health: the gastrointestinal potential of BSO
  • ​Diabetes: the anti-diabetic capacity of BSO
  • ​Skin Health: the ability of BSO to help with skin conditions
KETOKERRI BRAND
The KetoKerri Brand was created by Kerri Rivera, the Internationally Recognized Autism Author, to make Premium Products available at fair prices for the many people seeking health worldwide. Kerri advocates the Keto Diet and so the name KetoKerri was born. KetoKerri is Revolutionizing the Supplement Industry one product at a time.
ANCIENT ORIGINS
The history of the black cumin seed dates back to the time of the Pharaohs (1). It is mentioned in the Bible (2), was used by classical Greek physicians (3), has been used in the Arab world for thousands of years (4), has a rich tradition with historic Muslim physicians (2,5), and was mentioned by Maimonides (2).
NUTRIENT DENSE
Black seed oil is a significant source of essential fatty acids (EFAs), vitamins, minerals, proteins, and amino acids. It also contains hundreds of synergistic phytonutrients, including phytosterols, tocopherols, steroidal glycosides, and alkaloids (4,5,6,7).
VERSATILE
Black seed oil has been used to treat almost any disease or condition. These include asthma, eczema, inflammation, diabetes, influenza, rheumatism, gastrointestinal issues, cancer, hypertension, neurological issues, and many more (3,5,6).  It has also been used to promote general well-being (5).
ANTI-INFLAMMATORY
Black seed oil has
Anti-inflammatory Properties (6)
Antioxidant Properties (6,8)
Antihistamine Properties (5)

MICROBIAL DEFENSE
Black seed oil can act as an
Antibacterial agent (6,8)
Antifungal agent (6)
Antiparasitic agent (6)
HEART
HEALTH
Studies have shown the ability of black seed oil (Nigella sativa [NS]) to reduce blood pressure in animals (6). It has been used in traditional herbal medicine for this purpose for millennia (3,5,6).
 BRAIN HEALTH
The 2019 article “Nigella sativa L. (Black Cumin): A Promising Natural Remedy for Wide Range of Illnesses” reviewed 21 studies (9-31) exploring the potential of black seed oil (Nigella sativa [NS] and Thymoquinone [TQ]) in five specific neurological areas: Alzheimer’s disease, Parkinson’s disease, Depression and anxiety, Epilepsy, and Opioid Dependence and Tolerance. The review concluded NS and TQ held great promise for improvement in these areas (6).
GUT HEALTH
Animal and human studies have shown NS and TQ have broad gastroprotective and restorative potentials (3,5,6). These include treatments for Celiac disease, dyspepsia, and other common ailments.
DIABETES
Many of the properties exhibited by black seed oil have the potential to be helpful in the management and treatment of diabetes (6,7).  In particular it has the potential to reduce bad cholesterol and body weight (6).
 SKIN HEALTH
The 2015 article “Dermatological effects of Nigella sativa” examined all of the current studies and articles relating to NS and TQ as they relate to the skin. The article focused on ten areas of interest: the antibacterial properties, the antiviral properties, the antifungal properties, the antiparasitic properties, wound healing, psoriasis, acne vulgaris, allergic reactions, eczema, and skin cancer. The article concluded, “The published original research articles on the effects of N. sativa and its ingredients strongly indicate its pharmacological potential in dermatology” (47).

  KK BLACK SEED OIL
Characteristics and Potential Benefits of KK Black Seed Oil:
  • Source: the black seed oil in KK Black Seed Oil is virgin organic oil that is cold-pressed extracted without the use of solvents from the seeds of the Nigella sativa plant. It is then bottled in a cGMP/FDA compliant facility.
  • Nutrient Dense: It is a rich source of Omega-6 and Omega-9 essential fatty acids, vitamins, minerals, and synergistic phytonutrients.
  • Versatile: It has the potential to treat almost any disease or condition.
  • ​Anti-Inflammatory: It has the potential to act as an anti-inflammatory, antioxidant, and antihistamine.
  • ​Microbial Defense: It has the potential to act as an antibacterial, antifungal, and antiparasitic agent. 
  • ​Heart Heath: It has the potential to lower blood pressure and promote cardiovascular health.
  • ​Brain Health: It has the potential to help with neurological issues.
  • ​Gut Health: It has the potential to restore and protect the gastrointestinal tract.
  • ​Diabetes: Many of the properties of black seed oil can help with diabetes.
  • ​Skin Health: It has the potential to help with a wide range of skin issues.
Click the button below for an in-depth black seed oil article
DISCLAIMER
This page is intended for informational purposes only and not as a substitute for professional medical consultation, prevention, diagnosis, and treatment. The information provided is not intended to diagnose, treat, cure, or prevent any disease or condition. If you suspect you may have a disease or condition, you should consult a licensed healthcare practitioner. KK Black Seed Oil has not been independently studied or evaluated in relation to any of the information provided on this page.
FOOTNOTES
1. Padhye, S; Banerjee, S; Ahmad, A; Mohammad, R; Sarkar, FH (2008). From here to eternity-the secret of Pharaohs: Therapeutic potential of black cumin seeds and beyond. Cancer Ther.; 6, 495–510.
2. Botnick I, Xue W, Bar E, Ibdah M, Schwartz A, Joel DM, Lev E, Fait A, Lewinsohn E (2012). Distribution of primary and specialized metabolites in Nigella sativa seeds, a spice with vast traditional and historical uses. Molecules. 2012 Aug 24;17(9):10159-77.
3. Tavakkoli A, Mahdian V, Razavi BM, Hosseinzadeh H (2017). Review on Clinical Trials of Black Seed (Nigella sativa) and Its Active Constituent, Thymoquinone. J Pharmacopuncture. 2017 Sep;20(3):179-193.
4. Forouzanfar F, Bazzaz BSF, Hosseinzadeh H (2014). “Black cumin (Nigella sativa) and its constituent (thymoquinone): A review on antimicrobial effects,” Iranian Journal of Basic Medical Sciences, vol. 17, no. 12, pp. 929–938, 2014.
5. Darakhshan S, Bidmeshki Pour A, Hosseinzadeh Colagar A, Sisakhtnezhad S (2015). Thymoquinone and its therapeutic potentials. Pharmacol Res. 2015;95-96:138-58.
6. Yimer EM, Tuem KB, Karim A, Ur-Rehman N, Anwar F (2019). “Nigella sativa L. (Black Cumin): A Promising Natural Remedy for Wide Range of Illnesses,” Evidence-Based Complementary and Alternative Medicine, vol. 2019, Article ID 1528635, 16 pages, 2019.
7. Ahmad A, Husain A, Mujeeb M, Khan SA, Najmi AK, Siddique NA, Damanhouri ZA, Anwar F (2013). A review on therapeutic potential of Nigella sativa: A miracle herb. Asian Pac J Trop Biomed. 2013 May;3(5):337-52. doi: 10.1016/S2221-1691(13)60075-1. PMID: 23646296; PMCID: PMC3642442.
8. Ahmad I, Muneer KM, Tamimi IA, Chang ME, Ata MO, Yusuf N (2013). Thymoquinone suppresses metastasis of melanoma cells by inhibition of NLRP3 inflammasome. Toxicol. Appl. Pharmacol. 270 (1), 70–76.
9. Abdel-Zaher AO, Abdel-Rahman MS, Elwasei FM (2010). “Blockade of nitric oxide overproduction and oxidative stress by Nigella sativa oil attenuates morphine-induced tolerance and dependence in mice,” Neurochemical Research, vol. 35, no. 10, pp. 1557–1565, 2010.
10. Abdollahi Fard M, Shojaii A (2013). “Efficacy of iranian traditional medicine in the treatment of epilepsy,” BioMed Research International, vol. 2013, Article ID692751, 8 pages, 2013.
11. Abdul-Ameer N, Al-Harchan H (2010). Treatment of acne vulgaris with Nigella Sativa oil lotion. Iraq. Postgrad. Med.  J. 2, 140–143.
12. Abulfadl YS, El-Maraghy NN, Ahmed AAE, Nofal S, Badary OA (2018). “Protective effects of thymoquinone on Dgalactose and aluminum chloride induced neurotoxicity in rats: biochemical, histological and behavioral changes,” Neurological Research, vol. 40, no. 4, pp. 324–333, 2018.
13. Akhondian J, Kianifar H, Raoofziaee M, Moayedpour A, Toosi MB, Khajedaluee M (2011). “The effect of thymoquinone on intractable pediatric seizures (pilot study),” Epilepsy Research, vol. 93, no. 1, pp. 39–43, 2011.
14. Alhebshi AH, Gotoh M, Suzuki I (2013). “Thymoquinone protects cultured rat primary neurons against amyloid 𝛽-induced neurotoxicity,” Biochemical and Biophysical Research Communications, vol. 433, no. 4, pp. 362–367, 2013.
15. Alhebshi AH, Odawara A, Gotoh M, Suzuki I (2014). “Thymoquinone protects cultured hippocampal and human induced pluripotent stem cells-derived neurons against 𝛼-synuclein induced synapse damage,” Neuroscience Letters, vol. 570, pp. 126–131, 2014.
16. Ali BH, Blunden G (2003). Pharmacological and toxicological properties of Nigella sativa, Phytother. Res. 17 (2003) 299–305, PMID: 12722128.
17. Bano F, Ahmed A, Parveen T, Haider S (2014). “Anxiolytic and hyperlocomotive effects of aqueous extract of Nigella sativa L. seeds in rats,” Pakistan Journal of Pharmaceutical Sciences, vol. 27, no. 5, pp. 1547–1552, 2014.
18. Bin Sayeed MS, Shams T, Hossain SF, et al. (2014). “Nigella sativa L. seeds modulate mood, anxiety and cognition in healthy adolescent males,” Journal of Ethnopharmacology, vol. 152, no. 1, pp. 156–162, 2014.
19. Gilhotra N, Dhingra D (2011). “Thymoquinone produced antianxiety-like effects in mice through modulation of GABA and NO levels,” Pharmacological Reports, vol. 63, no. 3, pp. 660–669, 2011.
20. Hosseini M, Mohammadpour T, Karami R, Rajaei Z, Sadeghnia HR, Soukhtanloo M (2015). “Effects of the hydroalcoholic extract of Nigella Sativa on scopolamine-induced spatial memory impairment in rats and its possible mechanism,” Chinese Journal of Integrative Medicine, vol. 21, no. 6, pp. 438–444, 2015.
21. Mostafa R, Moustafa Y, Mirghani Z (2012). “Thymoquinone alone or in combination with phenobarbital reduces the seizure score and the oxidative burden in pentylenetetrazole-kindled rats,” Oxidants and Antioxidants in Medical Science, vol. 1, no. 3, pp. 185–192, 2012.
22. Norouzi F, Abareshi A, Anaeigoudari A, et al. (2016). “The effects of Nigella sativa on sickness behavior induced by lipopolysaccharide in male Wistar rats,” Avicenna Journal of Phytomedicine, vol. 6, no. 1, p. 104, 2016.
23. Perveen T, Haider S, Zuberi NA, Saleem S, Sadaf S, Batool Z (2014). “Increased 5-HT levels following repeated administration of Nigella sativa L. (black seed) oil produce antidepressant effects in rats,” Scientia Pharmaceutica, vol. 82, no. 1, pp. 161–170, 2014.
24. Radad K, Moldzio R, Taha M, Rausch WD (2009). “Thymoquinone protects dopaminergic neurons against MPP+ and rotenone,” Phytotherapy Research, vol. 23, no. 5, pp. 696–700, 2009.
25. Sahak MKA, Kabir N, Abbas G, Draman S, Hashim NH, Hasan Adli DS (2016). “The Role of Nigella sativa and its active constituents in learning and memory,” Evidence-Based Complementary and Alternative Medicine, vol. 2016, Article ID 6075679, 6 pages, 2016.
26. Sangi S, Ahmed SP, Channa MA, Ashfaq M, Mastoi SM (2008). “A new and novel treatment of opioid dependence: Nigella sativa 500mg,” Journal of AyubMedical College, vol. 20, no. 2, pp. 118–124, 2008.
27. Sayeed MSB, Asaduzzaman M, Morshed H, Hossain MM, Kadir MF, Rahman MR (2013). “The effect of Nigella sativa Linn. seed on memory, attention and cognition in healthy 14 Evidence-Based Complementary and Alternative Medicine human volunteers,” Journal of Ethnopharmacology, vol. 148, no. 3, pp. 780–786, 2013.
28. Sedaghat R, Roghani M, Khalili M (2014). “Neuroprotective effect of thymoquinone, the nigella sativa bioactive compound, in 6-hydroxydopamine-induced hemi-parkinsonian rat model,” Iranian Journal of Pharmaceutical Research, vol. 13, no. 1, pp. 227–234, 2014.
29. Seghatoleslam M, Alipour F, Shafieian R, et al. (2016). “The effects of Nigella sativa on neural damage after pentylenetetrazole induced seizures in rats,” Journal of Traditional and Complementary Medicine, vol. 6, no. 3, pp. 262–268, 2016.
30. Sharaf R, Elsayed MN, Mahran L (2014). “Neuroprotective effect of thymoquinone against lipopolysaccharide-induced Alzheimer’s disease in an animal model,” European Geriatric Medicine, vol. 5, no. 1, pp. S83–S158, 2014.
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32. Arafa ESA, Zhu Q, Shah ZI, et al. (2011). “Thymoquinone up-regulates PTEN expression and induces apoptosis in doxorubicin-resistant human breast cancer cells,” Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, vol. 706, no. 1-2, pp. 28–35, 2011.
33. Effenberger K, Breyer S, Schobert R (2010). “Terpene conjugates of the Nigella sativa seed-oil constituent thymoquinone with enhanced efficacy in cancer cells,” Chemistry &Biodiversity, vol. 7, no. 1, pp. 129–139, 2010.
34. Elkhoely A, Hafez HF, Ashmawy AM, et al. (2015). “Chemopreventive and therapeutic potentials of thymoquinone in HepG2 cells: Mechanistic perspectives,” Journal of Natural Medicines, vol. 69, no. 3, pp. 313–323, 2015.
35. Gali-Muhtasib H, Ocker M, Kuester D, et al. (2008). “Thymoquinone reduces mouse colon tumor cell invasion and inhibits tumor growth in murine colon cancer models,” Journal of Cellular and Molecular Medicine, vol. 12, no. 1, pp. 330–342, 2008.
36. Kabil N, Bayraktar R, Kahraman N, et al. (2018). “Thymoquinone inhibits cell proliferation, migration, and invasion by regulating the elongation factor 2 kinase (eEF-2K) signaling axis in triple negative breast cancer,” Breast Cancer Research and Treatment, vol. 171, no. 3, pp. 593–605, 2018.
37. Kou B, Kou Q, Ma B, et al. (2018). “Thymoquinone inhibits metastatic phenotype and epithelial-mesenchymal transition in renal cell carcinoma by regulating the LKB1/AMPK signaling pathway,” Oncology Reports, vol. 40, no. 3, pp. 1443–1450, 2018.
38. Kou B, Liu W, Zhao W, et al. (2017). “Thymoquinone inhibits epithelial-mesenchymal transition in prostate cancer cells by negatively regulating the TGF-𝛽/Smad2/3 signaling pathway,” Oncology Reports, vol. 38, no. 6, pp. 3592–3598, 2017.
39. Ng WK, Yazan LS, Ismail M (2011). “Thymoquinone from Nigella sativa was more potent than cisplatin in eliminating of SiHa cells via apoptosis with down-regulation of Bcl-2 protein,” Toxicology in Vitro, vol. 25, no. 7, pp. 1392–1398, 2011.
40. Periasamy VS, Athinarayanan J, Alshatwi AA (2016). “Anticancer activity of an ultrasonic nanoemulsion formulation of Nigella sativa L. essential oil on human breast cancer cells,” Ultrasonics Sonochemistry, vol. 31, pp. 449–455, 2016.
41. Salim EI (2010). “Cancer chemopreventive potential of volatile oil from black cumin seeds, Nigella sativa L., in a rat multi-organ carcinogenesis bioassay,” Oncology Letters, vol. 1, no. 5, pp. 913–924, 2010.
42. Salim EI, Fukushima S (2003). “Chemopreventive potential of volatile oil from black cumin (Nigella sativa L.) seeds against rat colon carcinogenesis,” Nutrition and Cancer, vol. 45, no. 2, pp. 195–202, 2003.
43. Schneider-Stock R, Fakhoury IH, Zaki AM, El-Baba CO, Gali-Muhtasib HU (2014). “Thymoquinone: fifty years of success in the battle against cancer models,” Drug Discovery Therapy, vol. 19, no. 1, pp. 18–30, 2014.
44. Shahin YR, Elguindy NM, Abdel Bary A, Balbaa M (2018). “The protective mechanism of Nigella sativa against diethylnitrosamine-induced hepatocellular carcinoma through its antioxidant effect and EGFR/ERK1/2 signaling,” Environmental Toxicology, vol. 33, no. 8, pp. 885–898, 2018.
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None of the products or statements on this website have been evaluated by the US Food and Drug Administration and are not intended to diagnose, treat, cure or prevent any disease or condition. If you suspect you may have a disease or condition, you should consult a licensed healthcare practitioner.
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