NalLife Co., Ltd.
FDA import alert and refusal historyRanot, ThailandFEI 3013910965
As of October 26, 2026, NalLife Co., Ltd. (Ranot, Thailand) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for organic soursop graviola leaves capsules, published by FDA on November 5, 2024, and has 3 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · DIETARYLBL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for NalLife Co., Ltd.
4 records, 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.DIETARYLBLNCONTACTNUTRIT LBLEntry 9LR-1176350-1Source
2024
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLLACKS FIRMNUTRIT LBLEntry 9LR-1175037-5Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLNCONTACTNUTRIT LBLEntry 9LR-1169099-3Source
- Import alert listingListed on Import Alert 99-39red listOrganic Soursop Graviola Leaves CapsulesSource
Refusal charges, in plain English
- DIETARYLBL3 refused lines
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- NUTRIT LBL3 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- NCONTACT2 refused lines
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- LACKS FIRM1 refused line
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
Questions about NalLife Co., Ltd.
- Is NalLife Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, NalLife Co., Ltd. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for organic soursop graviola leaves capsules; FDA published the listing on November 5, 2024.
- Has FDA refused shipments from NalLife Co., Ltd.?
- Yes. FDA refused 3 shipment lines from NalLife Co., Ltd. between November 21, 2024 and February 4, 2025. The most recent, on February 4, 2025, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as DIETARYLBL (not identified as a dietary supplement).
- Why did FDA refuse NalLife Co., Ltd.'s shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 3 lines) and NUTRIT LBL (nutrition information missing from label, 3 lines).
- What is NalLife Co., Ltd.'s FEI number?
- NalLife Co., Ltd.'s FDA Establishment Identifier (FEI) is 3013910965.
- Can shipments from NalLife Co., Ltd. still enter the U.S.?
- Shipments of organic soursop graviola leaves capsules from NalLife Co., Ltd. can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.