Herbal Doctor Remedies FDA Warning (2017)
Compiled by the Supplement Safety Data Team | Sourced from Official FDA Records on May 25, 2017
Executive Summary
The FDA issued a warning letter to Herbal Doctor Remedies on May 25, 2017 citing regulatory violations. Consumers who have purchased products from this company should exercise caution. The letter was issued by Los Angeles District Office.
Detailed Analysis
False Claims and Regulatory Violations
“This formula is very effective for treating . . . asthmatic cough . . ..”
“You can use this formula to prevent heat [sic] attack, [sic] by lowering cholesterol, LDL, and blood clots.”
“The most famous formula for treatment and prevention of glaucoma, cataract without surgery, conjunctivitis, hyperemia, blurred vision, pink eyes, photophobia and dry eyes.”
Potential Health Risks
Consumers should be aware of potential risks associated with products from Herbal Doctor Remedies.
Regulatory Context
“Indication: This formula helps improve lowering blood pressure, strengthen capillary action, cardiac pump . . ..”
“It helps . . . reduce painful swelling in the urinary tract. For pain, swelling and itching in the genital area, blood in the urine, redness in mouth, tongue and eyes. It is used for prostatits [sic], urethritis, cystitis, and inflammation of vagina.”
“The best herbal of choice for hyperthyroidism, substitute for . . . radioactive iodine and surgery.”
Key Entities Identified
Frequently Asked Questions
- What did the FDA find wrong with Herbal Doctor Remedies?
- The FDA issued a warning letter citing regulatory violations related to their products or manufacturing practices.
- Are Herbal Doctor Remedies products safe to use?
- Based on the FDA's findings, consumers should exercise caution. The company was found to have regulatory issues that may affect product safety.
- What should I do if I've used Herbal Doctor Remedies products?
- If you have used products from Herbal Doctor Remedies and experience any adverse effects, contact your healthcare provider immediately. You can also report adverse events to the FDA's MedWatch program.
Source Document
This report is based on an official FDA warning letter. The original document is a public record.
View Original FDA Warning Letter