Cold room to ambient bench.
Condensation can expose the label and print to moisture during transfers.



Custom identification labels for refrigerated samples, reagents, and pharmaceutical materials. Match the construction to your containers, storage temperatures, condensation, and cleaning requirements.
For sample tubes, reagent bottles, pharmaceutical vials, and process containers.

The label has to perform when a sample leaves the refrigerator, a reagent bottle is wiped down, or a chilled container is labeled. Those transitions can matter as much as the storage conditions.
Condensation can expose the label and print to moisture during transfers.
The adhesive must establish a bond under the conditions present when you apply the label.
Repeated retrieval, door-open cycles, and long storage periods make the full service history relevant.
The material and printing need to withstand the chemical and wiping method used in your process.
After storage, handling, and cleaning, the barcode must remain usable at the point of use.
Select every challenge in your workflow. Your selections help define the complete application.
Support identification across pharmaceutical fill-finish, cell therapy manufacturing, and laboratory & QC. Specify your actual temperature range; label performance depends on the recommended construction and application.
Maintain identification through refrigerated holding, controlled handling, cleaning, and transfer to the next production step.
Identify refrigerated materials between processing steps, including workflows that also involve frozen or cryogenic storage.
Keep samples and materials identifiable as they move between lab refrigerators, cold rooms, preparation areas, and analysis.
Match the adhesive to glass or plastic, container curvature, and the temperature and moisture present during application.
Include small diameters and edge-lift concerns.
Evaluate the facestock, printing, and protection through condensation, handling, and any chemical wipe-downs.
Include the actual printer and ribbon when printing onsite.
Consider cleanroom packaging, dispensing, and any sterilization exposure alongside refrigerated performance.
When a sample tube or reagent bottle leaves the refrigerator, condensation, handling, and disinfectant wipes can challenge its label. Peeling edges, smeared text, or an unreadable barcode can interrupt work and make identification harder.
CleanMark helps match the label to your container and process, so your team can identify, handle, and track materials throughout the workflow.

A technical contact and a clear application brief.
A proposed material, its TDS, and the rationale for the recommendation.
Evaluation samples with agreed supporting documentation.
An approved specification and agreed supply controls.
Share what you know. Only your first name, last name, and email are required.
Step 1 of 3 — Application
Anything left open can be discussed with our team.
Schedule a conversation about your refrigerated application →
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Include the actual storage range, the temperature and condition of the container when labeling, its material and shape, and what happens during removal, cleaning, and use. A storage temperature alone does not define the complete application.
Tell us whether the container is chilled and dry or has condensation on its surface. Adhesion during application must be evaluated separately from performance after the label is already attached.
The finished construction should be evaluated with the actual chemical, concentration, wiping method, and number of exposures. If you print onsite, include your printer and ribbon in that evaluation.
Share the container material and diameter, label dimensions, and barcode requirements. Tight curvature and limited surface area affect label fit, edge adhesion, and where the identification can be read or scanned.
These requirements can be considered together. Specify the packaging and handling needs, plus any sterilization process, so material selection and evaluation reflect the full workflow.
Include those exposures when requesting a recommendation. The label should be evaluated across the complete sequence, including temperature transitions and handling—not refrigeration alone.