Interphil Laboratories Inc
⚠️ High Risk
FEI: 3000293040 • Laguna • PHILIPPINES
FEI Number
3000293040
Location
Laguna
Country
PHILIPPINESAddress
Canlubang Industrial Estate, Bo., , Laguna, , Philippines
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/2/2025 | 54YDY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/2/2025 | 62MDY08MENTHOL (ANTI-PRURITIC) | Division of Northeast Imports (DNEI) | |
| 9/2/2025 | 61WDJ55TIOCONAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Interphil Laboratories Inc's FDA import refusal history?
Interphil Laboratories Inc (FEI: 3000293040) has 3 FDA import refusal record(s) in our database, spanning from 9/2/2025 to 9/2/2025.
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. Interphil Laboratories Inc's FEI number is 3000293040.
What types of violations has Interphil Laboratories Inc received?
Interphil Laboratories Inc has been cited for 2 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 Interphil Laboratories Inc come from?
All FDA import refusal data for Interphil Laboratories 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.