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Perilland

Quality

We would rather show you documents than describe ourselves. This page lists what we will publish, how manufacturers are chosen, and how we write about our products.

What we will publish before launch

Status as of October 2026: not yet published. Documents will appear on each product page.

The standards behind every bottle

Perilland is a brand of LIG Nutrition Inc. Before a product carries the Perilland name, its manufacturing has to meet these U.S. requirements.

The facility

  • Registered with the FDA as a food facility21 U.S.C. 350d
  • Follows current Good Manufacturing Practice (cGMP) for dietary supplements, checked by third-party audit21 CFR Part 111
  • Works under a written quality agreement with LIG Nutrition

Ingredients and batches

  • Every dietary ingredient is tested for identity when it arrives21 CFR 111.75
  • Every finished batch is tested for identity, strength, heavy metals (lead, arsenic, cadmium, mercury) and microbial limits, and released with a Certificate of Analysis21 CFR Part 111
  • Every bottle carries a lot number that traces back to its batch records

Labels and after the sale

  • A Supplement Facts panel in the FDA format21 CFR 101.36
  • Structure/function statements carry the FDA disclaimer and are notified to the FDA within 30 days of first marketing21 CFR 101.93
  • As importer, LIG Nutrition verifies its foreign suppliers under the Foreign Supplier Verification Program21 CFR Part 1, Subpart L
  • The label lists a U.S. contact, and serious adverse events are reported to the FDA within 15 business days21 U.S.C. 379aa-1

The FDA does not approve dietary supplements or certify manufacturers. Facility registration and cGMP compliance are legal requirements, not endorsements.

How we write about our products