Schwarzopf Henkel Corp
⚠️ Moderate Risk
FEI: 3003249556 • Dusseldorf • GERMANY
FEI Number
3003249556
Location
Dusseldorf
Country
GERMANYAddress
Henkel Strasse 67d-40191, , Dusseldorf, , 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
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).
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
LIST INGRE
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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
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.
COSM MISB2
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that its labeling is false or misleading in any particular.
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.
COSMETFPLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.
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).
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 |
|---|---|---|---|
| 8/26/2024 | 53FD04HAIR SHAMPOOS (COLORING) (HAIR COLORING PREPARATIONS) | 197COSM COLOR | Division of Southeast Imports (DSEI) |
| 3/8/2024 | 53EY06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | Division of Southeast Imports (DSEI) | |
| 11/10/2022 | 53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 197COSM COLOR | Division of Northern Border Imports (DNBI) |
| 6/16/2022 | 62WBY17ALUMINUM CHLORIDE ASTRINGENT/ANTI-PERSPIRANT) | Division of Northeast Imports (DNEI) | |
| 4/12/2017 | 53FD04HAIR SHAMPOOS (COLORING) (HAIR COLORING PREPARATIONS) | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 11/4/2015 | 53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 198COLOR LBLG | Division of Northern Border Imports (DNBI) |
| 12/27/2001 | 54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 218LIST INGRE | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Schwarzopf Henkel Corp's FDA import refusal history?
Schwarzopf Henkel Corp (FEI: 3003249556) has 7 FDA import refusal record(s) in our database, spanning from 12/27/2001 to 8/26/2024.
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. Schwarzopf Henkel Corp's FEI number is 3003249556.
What types of violations has Schwarzopf Henkel Corp received?
Schwarzopf Henkel Corp has been cited for 9 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 Schwarzopf Henkel Corp come from?
All FDA import refusal data for Schwarzopf Henkel Corp 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.