Interphil Laboratories Inc
FDA import alert and refusal historyLaguna, PhilippinesFEI 3000293040
As of October 26, 2026, Interphil Laboratories Inc is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 2, 2025, most often for product not listed with fda (NOT LISTED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NOT LISTED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Interphil Laboratories Inc
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NOT LISTEDUNAPPROVEDEntry AEK-7507398-9Source
Refusal charges, in plain English
- NOT LISTED1 refused line
Product not listed with FDA
The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Interphil Laboratories Inc
- Is Interphil Laboratories Inc on an FDA import alert?
- No listing for Interphil Laboratories Inc appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Philippines page.
- Has FDA refused shipments from Interphil Laboratories Inc?
- Yes. FDA refused 1 shipment line from Interphil Laboratories Inc on September 2, 2025. The most recent, on September 2, 2025, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NOT LISTED (product not listed with fda).
- Why did FDA refuse Interphil Laboratories Inc's shipments?
- The most frequent charges are NOT LISTED (product not listed with fda, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
- What is Interphil Laboratories Inc's FEI number?
- Interphil Laboratories Inc's FDA Establishment Identifier (FEI) is 3000293040.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.