Federation of State Medical Boards
Find the doctor's state board.
State bodies responsible for licensing doctors make up the Federation of State Medical Boards. Its directory links to each state board's own website.
Read the source pageRead the source. Check the name.
Use these pages for the rule or the record behind a claim.
These pages explain approval, rules for making medicine and checks on care. They do not show whether a proposed treatment helps memory.
Ask the doctor or other health professional for research on the exact medicine and memory claim. Read what was compared, what changed and what is still unknown.
Federation of State Medical Boards
State bodies responsible for licensing doctors make up the Federation of State Medical Boards. Its directory links to each state board's own website.
Read the source pageU.S. Food and Drug Administration
The FDA's pharmacy page directs readers to their state's licence search.
Read the source pageUS care access, as of September 2026.
U.S. Food and Drug Administration
The Food and Drug Administration (FDA) does not approve health care providers' offices.
Read the source pageU.S. Food and Drug Administration
With compounding, a pharmacy or doctor prepares or changes medicine to meet a patient's need. A medicine made this way does not have FDA approval or go through the FDA's checks before sale.
Read the source pageU.S. Food and Drug Administration
According to the FDA, a National Drug Code (NDC) does not mean a product has approval.
Read the source pageU.S. Food and Drug Administration
Semax is a peptide. Groups asked the FDA to allow it as an ingredient for making medicine, then took their requests back. The FDA still lists possible harms beside its semax entry.
Withdrawing those requests gave pharmacies no permission to use semax. FDA records checked for September 2026 show that it fails the federal ingredient rules that apply when pharmacies make medicine for individual patients.
For some injected peptides, the FDA warns that the body's defenses may react to them as something foreign. The FDA also raises concerns about unwanted material and too little research in people to judge the risks.
Read the source pageFederation of State Medical Boards
The Federation of State Medical Boards recommends that proper care go beyond picking an item from a treatment menu.
Read the source pageTelehealth.HHS.gov, U.S. Department of Health and Human Services
US guidance on telehealth licensing considers whether a doctor is permitted to practise at the patient's location during care.
Read the source pageOffice of the Law Revision Counsel, U.S. House of Representatives
Before a pharmacy gives you a prescription drug, a valid prescription is required under federal law. The prescription must come from a doctor or another health professional allowed to prescribe that drug.
Read the source pageU.S. Food and Drug Administration
The FDA describes unwanted material and wrong ingredient amounts as possible results of poor compounding.
Read the source pageNational Institutes of Health / US National Library of Medicine
MedlinePlus calls a severe allergic reaction life-threatening and directs people with severe symptoms to emergency care.
Read the source pageA public licence record does not rank the quality of care.
A page about approval does not show whether the medicine helps memory. Keep asking for research on that medicine and that use.
Bring the open questions to a visit