How many FDA warning letters has Herbal Dermals LLC FZ dba Gotucream received?

Argus HQ has recorded 1 FDA warning letter for Herbal Dermals LLC FZ dba Gotucream.

What FDA recalls has Herbal Dermals LLC FZ dba Gotucream issued?

Argus HQ has not recorded an FDA recall tied to Herbal Dermals LLC FZ dba Gotucream in our current dataset.

Is Herbal Dermals LLC FZ dba Gotucream FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 1 warning letter, 0 recalls, and 0 approval records for Herbal Dermals LLC FZ dba Gotucream. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Herbal Dermals LLC FZ dba Gotucream

Name: FDA Enforcement Actions Against Herbal Dermals LLC FZ dba Gotucream
Creator: Argus HQ
License: https://argushq.ai/methodology

Industry: pharmaceutical

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_warning_letter · unapproved_drug2026-06-17
Herbal Dermals LLC FZ dba Gotucream — Unapproved New Drugs/Misbranded (2026-06-17)

Frequently asked questions

How many FDA warning letters has Herbal Dermals LLC FZ dba Gotucream received?: Argus HQ has recorded 1 FDA warning letter for Herbal Dermals LLC FZ dba Gotucream.
What FDA recalls has Herbal Dermals LLC FZ dba Gotucream issued?: Argus HQ has not recorded an FDA recall tied to Herbal Dermals LLC FZ dba Gotucream in our current dataset.
Is Herbal Dermals LLC FZ dba Gotucream FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 1 warning letter, 0 recalls, and 0 approval records for Herbal Dermals LLC FZ dba Gotucream. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.