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HINDUSTAN UNILEVER LTD

⚠️ Moderate Risk

FEI: 3023651551 • Tinsukia • INDIA

FEI

FEI Number

3023651551

📍

Location

Tinsukia

🇮🇳

Country

INDIA
🏢

Address

Dag No 8,9,10,12,13,23, , Tinsukia, , India

Moderate Risk

FDA Import Risk Assessment

49.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
6
Unique Violations
4/17/2025
Latest Refusal
5/9/2023
Earliest Refusal

Score Breakdown

Violation Severity
52.9×40%
Refusal Volume
28.8×30%
Recency
85.3×20%
Frequency
25.7×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

1971×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

32001×

COSM MISB2

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that its labeling is false or misleading in any particular.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

Refusal History

DateProductViolationsDivision
4/17/2025
53EY06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
3200COSM MISB2
Division of Southeast Imports (DSEI)
9/11/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
473LABELING
Division of Northeast Imports (DNEI)
9/11/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
473LABELING
Division of Northeast Imports (DNEI)
9/3/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
Division of Northeast Imports (DNEI)
5/9/2023
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is HINDUSTAN UNILEVER LTD's FDA import refusal history?

HINDUSTAN UNILEVER LTD (FEI: 3023651551) has 5 FDA import refusal record(s) in our database, spanning from 5/9/2023 to 4/17/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. HINDUSTAN UNILEVER LTD's FEI number is 3023651551.

What types of violations has HINDUSTAN UNILEVER LTD received?

HINDUSTAN UNILEVER LTD has been cited for 6 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about HINDUSTAN UNILEVER LTD come from?

All FDA import refusal data for HINDUSTAN UNILEVER LTD is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.