BCG Baden-Baden Cosmetics Group GmbH
⚠️ Moderate Risk
FEI: 1000256921 • Baden-Baden, Baden-Wurttemberg • GERMANY
FEI Number
1000256921
Location
Baden-Baden, Baden-Wurttemberg
Country
GERMANYAddress
Im Rosengarten 7, , Baden-Baden, Baden-Wurttemberg, Germany
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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).
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).
INSAN BSE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health.
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.
WARNINGS
It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.
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)).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/26/2022 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | Division of West Coast Imports (DWCI) | |
| 8/7/2013 | 62WAY03ALUMINUM ACETATE (SOL) (ASTRINGENT/ANTI-PERSPIRANT) | New York District Office (NYK-DO) | |
| 10/1/2012 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | Florida District Office (FLA-DO) | |
| 3/9/2011 | 54YCL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 324NO ENGLISH | New Orleans District Office (NOL-DO) |
| 5/5/2010 | 62WBL17ALUMINUM CHLORIDE ASTRINGENT/ANTI-PERSPIRANT) | Southwest Import District Office (SWI-DO) | |
| 4/3/2002 | 53PC02COLLAGEN (COSMETIC RAW MATERIAL) | 2202INSAN BSE | Los Angeles District Office (LOS-DO) |
| 1/10/2002 | 66PAJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is BCG Baden-Baden Cosmetics Group GmbH's FDA import refusal history?
BCG Baden-Baden Cosmetics Group GmbH (FEI: 1000256921) has 7 FDA import refusal record(s) in our database, spanning from 1/10/2002 to 7/26/2022.
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. BCG Baden-Baden Cosmetics Group GmbH's FEI number is 1000256921.
What types of violations has BCG Baden-Baden Cosmetics Group GmbH received?
BCG Baden-Baden Cosmetics Group GmbH 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 BCG Baden-Baden Cosmetics Group GmbH come from?
All FDA import refusal data for BCG Baden-Baden Cosmetics Group GmbH 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.