Kanebo Cosmetics Co. Ltd.
⚠️ High Risk
FEI: 3001106818 • Tokyo, Tokyo • JAPAN
FEI Number
3001106818
Location
Tokyo, Tokyo
Country
JAPANAddress
1-14-10, NIHOMBASHI, KAYABACHO, Chuo-ku, Tokyo, 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
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).
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
DIRSEXMPT
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.
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.
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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
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).
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
POISONOUS
The article is subject to refusal of admission pursuant Section 801(a)(3) in that The cosmetic appears to bear or contain a poisonous or deleterious substance which may render it injurious to users under the conditions prescribed in the labeling thereof, or, under such conditions of use as are customary or usual.
HELD INSAN
The cosmetic appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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)).
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/4/2023 | 53CD02EYELINER (EYE MAKEUP PREPARATIONS) | 198COLOR LBLG | Division of West Coast Imports (DWCI) |
| 4/4/2023 | 53CD02EYELINER (EYE MAKEUP PREPARATIONS) | 198COLOR LBLG | Division of West Coast Imports (DWCI) |
| 9/3/2019 | 53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 9/3/2019 | 53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 9/3/2019 | 53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 9/3/2019 | 53LH01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
| 6/27/2019 | 53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 3260NO ENGLISH | Division of West Coast Imports (DWCI) |
| 8/1/2016 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 9/29/2015 | 29YYY02EMERGENCY DRINKING WATER (CIVIL DEFENSE), SOFT DRINKS AND WATERS, N.E.C. | 324NO ENGLISH | New Orleans District Office (NOL-DO) |
| 9/26/2011 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | New Orleans District Office (NOL-DO) | |
| 12/12/2007 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of West Coast Imports (DWCI) |
| 12/12/2007 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of West Coast Imports (DWCI) |
| 12/12/2007 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of West Coast Imports (DWCI) |
| 12/12/2007 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of West Coast Imports (DWCI) |
| 12/12/2007 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 2280DIRSEXMPT | Division of West Coast Imports (DWCI) |
| 5/24/2007 | 65LAJ99PROTECTANT N.E.C. | San Francisco District Office (SAN-DO) | |
| 5/24/2007 | 65LAJ99PROTECTANT N.E.C. | San Francisco District Office (SAN-DO) | |
| 5/24/2007 | 65LAJ99PROTECTANT N.E.C. | San Francisco District Office (SAN-DO) | |
| 5/24/2007 | 65LAJ99PROTECTANT N.E.C. | San Francisco District Office (SAN-DO) | |
| 5/24/2007 | 65LAJ99PROTECTANT N.E.C. | San Francisco District Office (SAN-DO) | |
| 12/22/2004 | 53EA02HAIR SPRAYS (AEROSOL FIXATIVES) (HAIR PREPARATIONS, NON-COLORING) | 251POISONOUS | Los Angeles District Office (LOS-DO) |
| 11/12/2004 | 53EA02HAIR SPRAYS (AEROSOL FIXATIVES) (HAIR PREPARATIONS, NON-COLORING) | 472NO ENGLISH | Los Angeles District Office (LOS-DO) |
| 11/12/2004 | 53EA02HAIR SPRAYS (AEROSOL FIXATIVES) (HAIR PREPARATIONS, NON-COLORING) | 310POISONOUS | Los Angeles District Office (LOS-DO) |
| 6/8/2004 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 12/31/2002 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 12/31/2002 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 12/31/2002 | 53LD02DEPILATORIES (SKIN CARE PREPARATIONS) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 12/31/2002 | 53LD02DEPILATORIES (SKIN CARE PREPARATIONS) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 12/31/2002 | 53LD02DEPILATORIES (SKIN CARE PREPARATIONS) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 7/1/2002 | 53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | 313HELD INSAN | Los Angeles District Office (LOS-DO) |
| 6/24/2002 | 53PD02COLLAGEN (COSMETIC RAW MATERIAL) | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 6/24/2002 | 53PD02COLLAGEN (COSMETIC RAW MATERIAL) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 6/24/2002 | 63VBL99DEPIGMENTOR N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 4/11/2002 | 53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/11/2002 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/11/2002 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/11/2002 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/11/2002 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 4/11/2002 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Kanebo Cosmetics Co. Ltd.'s FDA import refusal history?
Kanebo Cosmetics Co. Ltd. (FEI: 3001106818) has 39 FDA import refusal record(s) in our database, spanning from 4/11/2002 to 4/4/2023.
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. Kanebo Cosmetics Co. Ltd.'s FEI number is 3001106818.
What types of violations has Kanebo Cosmetics Co. Ltd. received?
Kanebo Cosmetics Co. Ltd. has been cited for 17 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 Kanebo Cosmetics Co. Ltd. come from?
All FDA import refusal data for Kanebo Cosmetics Co. Ltd. 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.