L'OREAL
⚠️ High Risk
FEI: 3012545541 • Clichy, Hauts-de-Seine • FRANCE
FEI Number
3012545541
Location
Clichy, Hauts-de-Seine
Country
FRANCEAddress
41 Rue Martre, , Clichy, Hauts-de-Seine, France
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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).
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).
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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) | Florida District Office (FLA-DO) | |
| 10/17/2016 | 53JI02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 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. | 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) | 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.