Supplement composition for supporting DNA repair and method of use

1. A method for enhancing DNA repair processes in a person in need thereof comprising orally administering a supplement composition to the person daily, said composition comprising in one dosage: from about 2,500 IU to about 10,000 IU of beta-carotene, from about 75 mg to about 500 mg of niacinamide, from about 5 mg to about 20 mg of zinc citrate, from about 250 mg to about 400 mg of inositol hexaphosphate, from about 100 mg to about 175 mg of a water extract of Uncaria tomentosa ; from about 175 mg to about 200 mg of trans-resveratrol, from about 5 mg to about 8 mg of an extract of Arabidopsis thaliana ; from about 25 mg to about 35 mg of an extract of cauliflower; and from about 20 mg to about 30 mg of an extract of Artemisia asiatica.

2. The method of claim 1 wherein the DNA repair process corrects DNA damage selected from the group consisting of single stranded DNA breaks, double stranded DNA breaks, cross-link damage, and base excision repair.

3. The method of claim 1 wherein the beta carotene is present in an amount of 5000 IU.

4. The method of claim 1 wherein the supplement composition is in the form of a tablet, a capsule, or a liquid.

5. The method of claim 1 wherein the extract of Uncaria tormentosa contains 4% to 15% carboxy alkyl esters.

6. The method of claim 1 wherein the supplement composition further comprises 8-oxoguanine glucosylase.

7. The method of claim 1 wherein the supplement composition further comprises a pharmaceutically acceptable medium.

8. The method of claim 7 wherein the pharmaceutically acceptable medium is selected from the group consisting of coloring, flavoring, diluting agents, emulsifying agents, suspending agents, ointment bases, pharmaceutical solvents, antioxidants and preservatives.

9. The method of claim 1 further comprising administering the supplement composition in conjunction with a dietary supplement.

10. The method of claim 1 wherein the supplement further comprises a diluting agent.

11. The method of claim 10 further comprising administering the supplement composition in conjunction with a dietary supplement.

12. The method of claim 10 wherein the diluting agent comprises calcium phosphate, calcium sulfate, lactose, kaolin, mannitol, sodium chloride, dry starch, powdered sugar, silica, or combinations thereof.

13. The method of claim 1 wherein the supplement composition further comprises a binder.

14. The method of claim 13 wherein the binder further comprises starch; gelatin; sugars, such as sucrose, glucose, dextrose, molasses, and lactose; natural and synthetic gums, such as acacia, sodium alginate, extract of Irish moss, panwar gum, ghatti gum, mucilage of isapol husks, carboxymethylcellulose, methylcellulose, polyvinylpyrrolidone, Veegum, microcrystalline cellulose, microcrystalline dextrose, amylose, and larch arabogalactan.

15. The method of claim 14 further comprising administering the supplement composition in conjunction with a dietary supplement.

16. The method of claim 7 wherein the pharmaceutically acceptable medium comprises dicalcium phosphate, microcrystalline cellulose, croscarmellose sodium, stearic acid, magnesium stearate, silica, and pharmaceutical glaze.

17. The method of claim 1 wherein administration of the supplement composition occurs twice daily.

18. The method of claim 17 further comprising administering the supplement composition in conjunction with a dietary supplement.

19. The method of claim 1 wherein the administration of the supplement composition is to a person having early indication of disorders related to DNA damages.

20. The method of claim 19 further comprising administering the supplement composition in conjunction with a dietary supplement.