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Supreme Henna Exports

FDA import alert and refusal historyAsangaon, IndiaFEI 2000045270

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Example subjectSupreme Henna Export added to Import Alert 16-129 (red list)

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As of October 26, 2026, Supreme Henna Exports is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 20, 2024, most often for color additive unsafe under section 721 (UNSAFE COL).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Henna · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Supreme Henna Exports

1 record, newest first. Each line links to the FDA page it came from.

2024

  1. Import refusal
    Refused, HennaUNSAFE COLEntry 9AJ-0861765-4
    Source

Refusal charges, in plain English

  • UNSAFE COL1 refused line

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Supreme Henna Exports

Is Supreme Henna Exports on an FDA import alert?
No listing for Supreme Henna Exports appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Supreme Henna Exports?
Yes. FDA refused 1 shipment line from Supreme Henna Exports on September 20, 2024. The most recent, on September 20, 2024, was henna, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Supreme Henna Exports's shipments?
The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
What is Supreme Henna Exports's FEI number?
Supreme Henna Exports's FDA Establishment Identifier (FEI) is 2000045270.

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Example subjectSupreme Henna Export added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.