Mitmitta (Cayenne Pepper)

Finding published by the FDA

Finding date: 9 July 2020.

Misbranding & Unapproved New Drugs

FDA finding date: 9 July 2020
Company: name not reproduced (no recognised company form)
Subject published by the FDA: Misbranding & Unapproved New Drugs
Published action: Recall
Programme: Foods

This official finding is dated and does not necessarily describe the product currently sold under this name. It does not constitute an analysis of its complete composition.

The subject and action are reproduced as published by the FDA, without generalisation to all batches or other products from the company.

Substances named in the FDA finding

No individual substance identified in the subject of this finding.

Substances named in the FDA finding do not constitute a complete composition. No quantity or dose is inferred.

Public register data after personal data protection

[
  {
    "action": "Recall",
    "company": "nom non repris (aucune forme de société reconnue)",
    "date": "2020-07-09",
    "fda_urls": [
      "https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sundial-herbal-products-recalling-products-attached-because-these-products-were-misbranded-products"
    ],
    "outcome": "",
    "product": "Mitmitta (Cayenne Pepper)",
    "program": "Foods",
    "source": "sundialherbs.com/sundial",
    "subject": "Misbranding & Unapproved New Drugs"
  }
]

Official source

View the FDA finding

Food and Drug Administration, Health Fraud Product Database. Constats officiels datés.

Domaine public (politique du site FDA)

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