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BCG Baden-Baden Cosmetics Group GmbH

⚠️ Moderate Risk

FEI: 1000256921 • Baden-Baden, Baden-Wurttemberg • GERMANY

FEI

FEI Number

1000256921

📍

Location

Baden-Baden, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Im Rosengarten 7, , Baden-Baden, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

41.5
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

7
Total Refusals
7
Unique Violations
7/26/2022
Latest Refusal
1/10/2002
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
33.5×30%
Recency
30.7×20%
Frequency
3.4×10%
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

1185×

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).

752×

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).

22021×

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.

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.

3441×

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.

3241×

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)).

161×

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

DateProductViolationsDivision
7/26/2022
62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C.
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
8/7/2013
62WAY03ALUMINUM ACETATE (SOL) (ASTRINGENT/ANTI-PERSPIRANT)
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
10/1/2012
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
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)
118NOT LISTED
16DIRECTIONS
344WARNINGS
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.