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PreCHEK 10 Multi Urine Drug Test Cup
(CLIA Waived)
  • One step

  • FDA approved and CLIA waived

  • 24 months shelf life

  • Perfect for self testing at home and office

  • Easy to read results

  • Results within 5 minutes

Available in stock.


Test Item

Test per Box









25 tests

25 tests

* For any customized combinations, adulteration strips, label design and mold design, please be free to contact us.


PreCHEK 10 Multi Urine Drug Test Cup is a lateral flow chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine at a cut-off concentration.


The product is FDA approved, CLIA Waived and CE marked, It is ideal for use in workplace screening, forensics, emergencies, detoxification treatment, addiction management treatment, transport authorities and custom and home use. 

How to use
result reading

Test must be in room temperature (50.0℉ ~86.0℉/10 ºC ~30 ºC)

  1. Remove the test cup from the foil pouch by tearing at the notch and use it as soon as possible.

  2. Open the cap of the test cup and urinate directly into the test cup.

  3. Fill the cup to above “MIN Volume” mark.

  4. Wipe off any splashes or spills that may be on the outside of this cup.

  5. After the urine has been collected, re-cap the cup and place the test cup on a flat surface.

  6. Read temperature immediately to verify that urine temperature is within the acceptable range: 90ºF-100ºF (32℃~38℃).

  7. Start the timer. Peel the label from right to left and read the result within 5 minutes. Do not read results after 5 minutes.

Read the result

Positive (+)

One colored line appears in the control line region (C). No line appears in the test line region (T). This positive result indicates that the drug concentration exceeds the detectable level.


Negative (-)

Two lines appear. One colored line should be in the control line region (C), and another apparent colored line should be in the test line region (T). This negative result indicates that the drug concentration is below the detectable level.



Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test using a new test. If the problem persists, discontinue using the lot immediately and contact your local distributor with the lot number.