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Lab Naprovid

FDA import alert and refusal historySonora, MexicoFEI 3031120658

Recorded by FDA as LAB NAPROVID

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Example subjectLab Naprovi added to Import Alert 16-129 (red list)

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As of October 26, 2026, Lab Naprovid (Sonora, Mexico) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for contra reumas suplemento alimenticio (against rheumatism dietary supplement), published by FDA on June 22, 2026, and has 2 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Herbals & botanicals (not teas), n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lab Naprovid

3 records, newest first. Each line links to the FDA page it came from.

2026

  1. Import alert listing
    Listed on Import Alert 54-16red listContra Reumas Suplemento Alimenticio (Against Rheumatism Dietary Supplement)
    Source

2025

  1. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.NO ENGLISHNCONTACTNUTRIT LBLUNAPPROVEDEntry AEK-7329740-8
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHEntry SCS-1687813-9
    Source

Refusal charges, in plain English

  • NO ENGLISH2 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NCONTACT1 refused line

    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.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • 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 Lab Naprovid

Is Lab Naprovid on an FDA import alert?
Yes. As of October 26, 2026, Lab Naprovid is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for contra reumas suplemento alimenticio (against rheumatism dietary supplement); FDA published the listing on June 22, 2026.
Has FDA refused shipments from Lab Naprovid?
Yes. FDA refused 2 shipment lines from Lab Naprovid on August 13, 2025. The most recent, on August 13, 2025, was herbals & botanicals (not teas), n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Lab Naprovid's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 2 lines) and NCONTACT (no u.s. adverse event contact on supplement label, 1 line).
What is Lab Naprovid's FEI number?
Lab Naprovid's FDA Establishment Identifier (FEI) is 3031120658.
Can shipments from Lab Naprovid still enter the U.S.?
Shipments of contra reumas suplemento alimenticio (against rheumatism dietary supplement) from Lab Naprovid can be detained without physical examination under Import Alert 54-16; 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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Example subjectLab Naprovi added to Import Alert 16-129 (red list)

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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.