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UNILEVER BANGLADESH LIMITED

⚠️ Moderate Risk

FEI: 3006160626 • CHITTAGONG • BANGLADESH

FEI

FEI Number

3006160626

📍

Location

CHITTAGONG

🇧🇩

Country

BANGLADESH
🏢

Address

51, KALURGHAT HEAVY I/A, , CHITTAGONG, , Bangladesh

Moderate Risk

FDA Import Risk Assessment

41.3
LowModerateHighCritical

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

Statistics

10
Total Refusals
12
Unique Violations
10/13/2023
Latest Refusal
4/18/2007
Earliest Refusal

Score Breakdown

Violation Severity
52.3×40%
Refusal Volume
38.6×30%
Recency
40.9×20%
Frequency
6.1×10%
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

1184×

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).

4714×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

1973×

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).

3362×

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.

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

4722×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

4732×

LABELING

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

4752×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

752×

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).

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.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

3241×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

Refusal History

DateProductViolationsDivision
10/13/2023
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
3881COSMETFPLA
Division of Northeast Imports (DNEI)
6/15/2016
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
473LABELING
475COSMETLBLG
Division of Northeast Imports (DNEI)
6/15/2016
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
473LABELING
475COSMETLBLG
Division of Northeast Imports (DNEI)
3/4/2011
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
3/4/2011
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
7/9/2007
53EY06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
471CSTIC LBLG
Southwest Import District Office (SWI-DO)
7/9/2007
53EY06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
471CSTIC LBLG
Southwest Import District Office (SWI-DO)
6/22/2007
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
16DIRECTIONS
336INCONSPICU
472NO ENGLISH
Southwest Import District Office (SWI-DO)
6/22/2007
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
16DIRECTIONS
336INCONSPICU
472NO ENGLISH
Southwest Import District Office (SWI-DO)
4/18/2007
31KGH99TEA, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

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

UNILEVER BANGLADESH LIMITED (FEI: 3006160626) has 10 FDA import refusal record(s) in our database, spanning from 4/18/2007 to 10/13/2023.

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. UNILEVER BANGLADESH LIMITED's FEI number is 3006160626.

What types of violations has UNILEVER BANGLADESH LIMITED received?

UNILEVER BANGLADESH LIMITED has been cited for 12 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 UNILEVER BANGLADESH LIMITED come from?

All FDA import refusal data for UNILEVER BANGLADESH 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.