US2022110918A1PendingUtilityA1

Compositions and methods for treatment of skin-related diseases and promoting dermatological health

Assignee: SCRIPT ESSENTIALS LLCPriority: Oct 9, 2020Filed: Oct 12, 2021Published: Apr 14, 2022
Est. expiryOct 9, 2040(~14.2 yrs left)· nominal 20-yr term from priority
Inventors:Suzy Cohen
C12Y 115/00A61P 17/00A23L 33/135A23L 33/15A23L 33/16A23L 33/105A23L 33/10A61K 35/747A61K 36/87A61K 33/30A61K 31/375A61K 31/4188A61K 38/446A61K 47/44
60
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present disclosure relates to dietary supplements, for improving dermatological health. In embodiments, the composition is comprised of D-Biotin, grape seed extract, superoxide dismutase, zinc, Vitamin C, Lactobacillus Plantarum, Lactobacillus Reuteri, Lactobacillus Rhamnosus , or combinations/sub-combinations thereof.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for treating a skin-related condition by administering an effective amount of a composition to a patient, wherein the composition comprises:
 between about 1,000 mcg and about 3,000 mcg of D-Biotin;   between about 50 mg and about 300 mg of a first blend, comprising:
 grape seed extract; 
 superoxide dismutase; 
 Zinc; and 
 Vitamin C; 
   between 1 Billion CFU/g and 5 Billion CFU/g of a second blend, comprising:
   Lactobacillus Plantarum;    
   Lactobacillus Reuteri ; and 
   Lactobacillus Rhamnosus.    
   
     
     
         2 . The method of  claim 1 , wherein the composition is administered orally in the form of a capsule. 
     
     
         3 . The method of  claim 1 , wherein the first blend of grape seed extract, superoxide dismutase, Zinc and Vitamin C comprises about 150 mg of the composition administered to the patient. 
     
     
         4 . The method of  claim 1 , wherein the grape seed extract in the first blend is a French grape seed extract. 
     
     
         5 . The method of  claim 1 , wherein the superoxide dismutase in the first blend if derived from melon. 
     
     
         6 . The method of  claim 1 , wherein the second blend of  Lactobacillus Plantarum, Lactobacillus Reuteri  and  Lactobacillus Rhamnosus  comprises about 3 Billion CFU/g of the composition administered to the patient. 
     
     
         7 . The method of  claim 1 , wherein the D-Biotin comprises about 2,000 mcg of the composition administered to the patient. 
     
     
         8 . The method of  claim 1 , wherein the composition administered to the patient does not comprise additives selected from the group consisting of gluten, wheat, egg, peanuts, tree nuts, dairy, sugar, com, soy, artificial colors, preservatives, fish and shellfish. 
     
     
         9 . The method of  claim 1 , wherein the composition administered to the patient further comprises at least one palatability agent. 
     
     
         10 . The method of  claim 9 , wherein the palatability agent is selected from the group consisting of plant oils, plant hydrolysates, yeast, and yeast hydrolysates. 
     
     
         11 . A method for treating a skin-related disease, comprising:
 administering an effective amount of a composition to a patient, wherein the composition comprises:   about 2,000 mcg of D-Biotin;   about 150 mg of a first blend, wherein the first blend comprises:
 grape seed extract; 
 superoxide dismutase; 
 Zinc; and 
 Vitamin C; 
   about 3 Billion CFU/g of a second blend, wherein the second blend comprises:
   Lactobacillus Plantarum;    
   Lactobacillus Reuteri ; and 
   Lactobacillus Rhamnosus.    
   
     
     
         12 . The method of  claim 11 , wherein the composition is administered orally in the form of a capsule, tablet, lozenge or powder. 
     
     
         13 . The method of  claim 11 , wherein the grape seed extract in the first blend is a French grape seed extract. 
     
     
         14 . The method of  claim 11 , wherein the superoxide dismutase in the first blend if derived from melon. 
     
     
         15 . The method of  claim 11 , wherein the composition administered to the patient does not comprise additives selected from the group consisting of gluten, wheat, egg, peanuts, tree nuts, dairy, sugar, com, soy, artificial colors, preservatives, fish and shellfish. 
     
     
         16 . The method of  claim 11 , wherein the composition administered to the patient further comprises at least one palatability agent. 
     
     
         17 . The method of  claim 16 , wherein the palatability agent is selected from the group consisting of plant oils, plant hydrolysates, yeast, and yeast hydrolysates. 
     
     
         18 . The method of  claim 11 , wherein the composition is administered orally to the patient between 1-4 times each day. 
     
     
         19 . The method of  claim 11 , wherein the skin-related disease is selected from the group consisting of skin cancer, acne, eczema, psoriasis, rosacea, ichthyosis, vitiligo, hives, dermatitis, and seborrheic dermatitis.

Join the waitlist — get patent alerts

Track US2022110918A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.