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L'OREAL

⚠️ High Risk

FEI: 3012545541 • Clichy, Hauts-de-Seine • FRANCE

FEI

FEI Number

3012545541

📍

Location

Clichy, Hauts-de-Seine

🇫🇷

Country

FRANCE
🏢

Address

41 Rue Martre, , Clichy, Hauts-de-Seine, France

High Risk

FDA Import Risk Assessment

54.2
LowModerateHighCritical

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

Statistics

27
Total Refusals
7
Unique Violations
2/11/2023
Latest Refusal
8/18/2007
Earliest Refusal

Score Breakdown

Violation Severity
70.3×40%
Refusal Volume
53.6×30%
Recency
41.4×20%
Frequency
17.4×10%
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

7517×

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).

1189×

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).

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

4731×

LABELING

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

4751×

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.

4711×

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.

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.

Refusal History

DateProductViolationsDivision
2/11/2023
66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Southeast Imports (DSEI)
4/4/2022
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Southeast Imports (DSEI)
5/16/2020
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
3280FRNMFGREG
Division of Southeast Imports (DSEI)
9/24/2019
66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Southeast Imports (DSEI)
5/26/2017
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
118NOT LISTED
Division of Southeast Imports (DSEI)
5/26/2017
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
118NOT LISTED
Division of Southeast Imports (DSEI)
10/17/2016
53JI02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
75UNAPPROVED
Florida District Office (FLA-DO)
10/17/2016
53JI02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
75UNAPPROVED
Florida District Office (FLA-DO)
2/1/2016
66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
62WBL05ZIRCONIUM
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL05HOMOSALATE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL05HOMOSALATE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL05HOMOSALATE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
66PBL07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
62WBL05ZIRCONIUM
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
62WBL05ZIRCONIUM
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
62WBL05ZIRCONIUM
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
62WBL05ZIRCONIUM
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2013
62WBL05ZIRCONIUM
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/14/2012
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
3741FRNMFGREG
Division of West Coast Imports (DWCI)
8/18/2007
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
475COSMETLBLG
New Orleans District Office (NOL-DO)
8/18/2007
53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
473LABELING
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is L'OREAL's FDA import refusal history?

L'OREAL (FEI: 3012545541) has 27 FDA import refusal record(s) in our database, spanning from 8/18/2007 to 2/11/2023.

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. L'OREAL's FEI number is 3012545541.

What types of violations has L'OREAL received?

L'OREAL has been cited for 7 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 L'OREAL come from?

All FDA import refusal data for L'OREAL 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.