SkinMedica, Inc.
⚠️ Moderate Risk
FEI: 3010164187 • Carlsbad, CA • UNITED STATES
FEI Number
3010164187
Location
Carlsbad, CA
Country
UNITED STATESAddress
5770 Armada Dr, , Carlsbad, CA, United States
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
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).
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).
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.
AGR RX
The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/5/2017 | 64XBL03BENZOYL PEROXIDE (KERATOLYTIC) | 179AGR RX | Division of Southeast Imports (DSEI) |
| 2/27/2017 | 66PBJ07OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN) | Division of Southeast Imports (DSEI) | |
| 2/27/2017 | 65LBL11TITANIUM DIOXIDE (PROTECTANT) | Division of Southeast Imports (DSEI) | |
| 2/27/2017 | 64XBL03BENZOYL PEROXIDE (KERATOLYTIC) | Division of Southeast Imports (DSEI) | |
| 2/27/2017 | 64XBL03BENZOYL PEROXIDE (KERATOLYTIC) | Division of Southeast Imports (DSEI) | |
| 6/11/2015 | 65LBL11TITANIUM DIOXIDE (PROTECTANT) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/11/2015 | 50MGY29ZINC OXIDE | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/11/2015 | 53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SkinMedica, Inc.'s FDA import refusal history?
SkinMedica, Inc. (FEI: 3010164187) has 8 FDA import refusal record(s) in our database, spanning from 6/11/2015 to 6/5/2017.
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. SkinMedica, Inc.'s FEI number is 3010164187.
What types of violations has SkinMedica, Inc. received?
SkinMedica, Inc. has been cited for 4 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 SkinMedica, Inc. come from?
All FDA import refusal data for SkinMedica, Inc. 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.