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COSRX INC

⚠️ High Risk

FEI: 3012258694 • Seongnam, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3012258694

📍

Location

Seongnam, Gyeonggi

🇰🇷
🏢

Address

Bundangemtawo, 8 Gumi-Ro; Bundang, Seongnam, Gyeonggi, South Korea

High Risk

FDA Import Risk Assessment

65.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

33
Total Refusals
11
Unique Violations
11/13/2025
Latest Refusal
4/4/2016
Earliest Refusal

Score Breakdown

Violation Severity
63.5×40%
Refusal Volume
56.7×30%
Recency
96.6×20%
Frequency
34.3×10%
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

7514×

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).

50812×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

1187×

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).

32807×

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.

3414×

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).

4722×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

4711×

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.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

22801×

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.

Refusal History

DateProductViolationsDivision
11/13/2025
79FRODRESSING, WOUND, DRUG
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Northeast Imports (DNEI)
11/13/2025
64XAL06SALICYLIC ACID (KERATOLYTIC)
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/2/2025
79NACDRESSING, WOUND, HYDROPHILIC
508NO 510(K)
Division of Southeast Imports (DSEI)
5/31/2024
53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
75UNAPPROVED
Division of West Coast Imports (DWCI)
1/11/2022
79NADDRESSING, WOUND, OCCLUSIVE
341REGISTERED
Division of West Coast Imports (DWCI)
8/23/2021
79NADDRESSING, WOUND, OCCLUSIVE
118NOT LISTED
341REGISTERED
Division of West Coast Imports (DWCI)
8/12/2021
53LG08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS)
508NO 510(K)
Division of West Coast Imports (DWCI)
8/12/2021
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
508NO 510(K)
Division of West Coast Imports (DWCI)
8/12/2021
79NADDRESSING, WOUND, OCCLUSIVE
508NO 510(K)
Division of West Coast Imports (DWCI)
8/12/2021
79NACDRESSING, WOUND, HYDROPHILIC
508NO 510(K)
Division of West Coast Imports (DWCI)
7/27/2021
53LY03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
508NO 510(K)
Division of West Coast Imports (DWCI)
7/21/2021
53LY03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
508NO 510(K)
Division of West Coast Imports (DWCI)
6/9/2021
79NADDRESSING, WOUND, OCCLUSIVE
508NO 510(K)
Division of Southeast Imports (DSEI)
1/12/2021
79NACDRESSING, WOUND, HYDROPHILIC
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
3/2/2020
53LF01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/23/2020
53LY03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Northeast Imports (DNEI)
7/24/2019
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/11/2019
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
12/6/2018
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southwest Imports (DSWI)
10/1/2018
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
7/3/2018
53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/23/2018
53JK01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Division of West Coast Imports (DWCI)
5/23/2018
53JK01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Division of West Coast Imports (DWCI)
5/23/2018
53JK01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Division of West Coast Imports (DWCI)
5/23/2018
53JK01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Division of West Coast Imports (DWCI)
8/8/2017
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
336INCONSPICU
Division of Southeast Imports (DSEI)
8/8/2017
79NACDRESSING, WOUND, HYDROPHILIC
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
5/15/2017
53LY03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
2280DIRSEXMPT
75UNAPPROVED
Division of West Coast Imports (DWCI)
12/8/2016
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Seattle District Office (SEA-DO)
12/8/2016
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Seattle District Office (SEA-DO)
7/13/2016
53LY03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
475COSMETLBLG
Los Angeles District Office (LOS-DO)
6/6/2016
65LBL99PROTECTANT N.E.C.
3280FRNMFGREG
472NO ENGLISH
75UNAPPROVED
Los Angeles District Office (LOS-DO)
4/4/2016
64XBL06SALICYLIC ACID (KERATOLYTIC)
472NO ENGLISH
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is COSRX INC's FDA import refusal history?

COSRX INC (FEI: 3012258694) has 33 FDA import refusal record(s) in our database, spanning from 4/4/2016 to 11/13/2025.

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. COSRX INC's FEI number is 3012258694.

What types of violations has COSRX INC received?

COSRX INC has been cited for 11 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 COSRX INC come from?

All FDA import refusal data for COSRX 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.