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Impression Cosmetics

FDA import alert and refusal historyNew Delhi, IndiaFEI 3016626112

Recorded by FDA as IMPRESSION COSMETICS

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Example subjectImpression Cosmetic added to Import Alert 16-129 (red list)

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As of October 26, 2026, Impression Cosmetics is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 11, 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 Impression Cosmetics

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

2024

  1. Import refusal
    Refused, HennaUNSAFE COLEntry 799-4409123-1
    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 Impression Cosmetics

Is Impression Cosmetics on an FDA import alert?
No listing for Impression Cosmetics 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 Impression Cosmetics?
Yes. FDA refused 1 shipment line from Impression Cosmetics on December 11, 2024. The most recent, on December 11, 2024, was henna, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Impression Cosmetics's shipments?
The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
What is Impression Cosmetics's FEI number?
Impression Cosmetics's FDA Establishment Identifier (FEI) is 3016626112.

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Example subjectImpression Cosmetic 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.