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HINDUSTAN UNILEVER LIMITED

⚠️ High Risk

FEI: 3031311125 • Tinsukia • INDIA

FEI

FEI Number

3031311125

📍

Location

Tinsukia

🇮🇳

Country

INDIA
🏢

Address

Dag No 21 Of 122 Fs Gra, , Tinsukia, , India

High Risk

FDA Import Risk Assessment

59.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

12
Total Refusals
5
Unique Violations
10/7/2024
Latest Refusal
12/11/2019
Earliest Refusal

Score Breakdown

Violation Severity
82.0×40%
Refusal Volume
41.3×30%
Recency
60.7×20%
Frequency
24.9×10%
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

758×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

1974×

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.

38811×

COSMETFPLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.

Refusal History

DateProductViolationsDivision
10/7/2024
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Northeast Imports (DNEI)
10/2/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
Division of Northeast Imports (DNEI)
10/2/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
Division of Northeast Imports (DNEI)
9/27/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
3200COSM MISB2
3881COSMETFPLA
Division of Southeast Imports (DSEI)
9/11/2024
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
75UNAPPROVED
Division of Northeast Imports (DNEI)
9/3/2024
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/17/2024
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
Division of Northern Border Imports (DNBI)
5/2/2023
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
75UNAPPROVED
Division of Northeast Imports (DNEI)
5/2/2023
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
75UNAPPROVED
Division of Northeast Imports (DNEI)
5/2/2023
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
75UNAPPROVED
Division of Northeast Imports (DNEI)
4/7/2023
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
75UNAPPROVED
Division of Northeast Imports (DNEI)
12/11/2019
63RBJ04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
75UNAPPROVED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

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

HINDUSTAN UNILEVER LIMITED (FEI: 3031311125) has 12 FDA import refusal record(s) in our database, spanning from 12/11/2019 to 10/7/2024.

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 LIMITED's FEI number is 3031311125.

What types of violations has HINDUSTAN UNILEVER LIMITED received?

HINDUSTAN UNILEVER LIMITED has been cited for 5 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 LIMITED come from?

All FDA import refusal data for HINDUSTAN UNILEVER LIMITED 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.