Lot traceability: matching a vial to its record

What the identifier on a vial label is for, how it links to a published analytical record, and how a laboratory keeps that link intact from receipt onward.

Research-use scope. This page covers labels, identifiers, and records only. It is not for use in people or animals, contains no handling or procedural guidance, and does not replace the receiving laboratory's own procedures.

Why the lot identifier is the key

A product name describes a material in general. A lot identifier describes one production batch of it. Analytical testing is performed on samples from a lot, so every meaningful record (a certificate of analysis, a verification entry, a receiving log line) hangs off the lot identifier, not the name. Two vials with the same name and different lots are, for documentation purposes, two different things.

Reading an Arctic Lab Supply lot code

Lot identifiers on Arctic Lab Supply labels follow a compact pattern: a short material prefix, a production period, and a sequence letter. For example, BCP-2502-B is the second lot (B) of a BPC-157 production period coded 2502, and RT-2502-A is the first lot of an AL-RT period with the same code. The strength is printed separately on the label and stated separately on the report; a lot code alone does not imply a strength.

Label fieldPurposeWhere it must match
Material nameIdentifies the substance in the catalog's public nomenclature.The sample identity line of the report and the product page.
Labeled strengthThe nominal amount per sealed vial.The strength stated on the report. A 5 mg report does not describe a 10 mg vial.
Lot identifierThe production batch the vial belongs to.The lot line of the report and the entry in the COA library.
Research-use statementStates the intended laboratory-only scope of the material.Consistent with the supplier's published research standards.

From label to record in four steps

  1. At receipt, write down the material name, labeled strength, and lot identifier for each container, along with the date and the person receiving it.
  2. Open the batch COA library and find the entry whose product, strength, and lot all match. Partial matches do not count.
  3. Follow the entry's verification link to the testing laboratory and confirm the certificate number corresponds to the same lot and date.
  4. Store the PDF, the certificate number, and the verification date with the receiving record so the chain can be reproduced later without the website.
One report, one lot. Arctic Lab Supply never reuses an analytical report across products, strengths, or lots. If a product page or the library shows no report for the lot you received, that lot is currently undocumented, and the catalog says so. A report for an earlier lot of the same material is historical context, not evidence about the lot in hand.

What breaks traceability

Questions to ask a supplier

Which lot was this vial filled from? Where is the published report for that exact lot and strength? Can the issuing laboratory verify the certificate number? When a supplier can answer all three with documents rather than assurances, the vial is traceable. When they cannot, record the gap and classify the material accordingly under the laboratory's own procedures.

Related documentation