Kose Corporation
⚠️ High Risk
FEI: 1000233216 • Chuo, Tokyo • JAPAN
FEI Number
1000233216
Location
Chuo, Tokyo
Country
JAPANAddress
(Kabu) Kose, 3 Chome 6-2; Nihonbashi, Chuo, Tokyo, Japan
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
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.
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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).
DRUG NAME
The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/10/2025 | 53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/25/2023 | 53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 2/7/2023 | 53ED99OTHER HAIR PREPARATIONS, NON-COLORING), N.E.C. | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 1/17/2023 | 53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 1/17/2023 | 53LY99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 12/9/2019 | 53YD99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 12/9/2019 | 53CH01EYEBROW PENCIL (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 12/9/2019 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 12/9/2019 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 12/9/2019 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 12/9/2019 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 9/3/2019 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 9/3/2019 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 9/3/2019 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 8/31/2015 | 66PAO99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | Cincinnati District Office (CIN-DO) | |
| 4/8/2015 | 53LC08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 3/24/2015 | 53LC08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 12/9/2014 | 53LY99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 11/12/2014 | 53LD08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 10/29/2014 | 53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 4/21/2011 | 66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 483DRUG NAME | New York District Office (NYK-DO) |
| 8/25/2005 | 53LC09SKIN FRESHENERS (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 8/25/2005 | 53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 9/18/2004 | 65LBL99PROTECTANT N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/18/2004 | 65LBL11TITANIUM DIOXIDE (PROTECTANT) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Kose Corporation's FDA import refusal history?
Kose Corporation (FEI: 1000233216) has 25 FDA import refusal record(s) in our database, spanning from 9/18/2004 to 2/10/2025.
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. Kose Corporation's FEI number is 1000233216.
What types of violations has Kose Corporation received?
Kose Corporation has been cited for 8 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 Kose Corporation come from?
All FDA import refusal data for Kose Corporation 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.