Single Urine Drug Test Dip Card (Neutral Package)



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One step
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FDA approved
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24 months shelf life
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Perfect for workplace screening, insurance testing and forensic use purpose
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Easy to read results
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Results within 5 minutes
Model
Test Item
Test per Box
N-TH501
N-CO501
N-BA501
N-MO501
N-OP501
N-AM501
N-AM501-2
N-MD501
N-FT501
N-K2501
THC 50ng/mL
COC 300ng/mL
BAR 300ng/mL
MOP 300ng/mL
OPI 2000ng/mL
AMP 1000ng/mL
AMP 500ng/mL
MDMA 500ng/mL
FTY 20ng/mL
K2 50ng/mL
25 tests
25 tests
25 tests
25 tests
25 tests
25 tests
25 tests
25 tests
25 tests
25 tests
* For label design and mold design, please be free to contact us.
Specifications
Single urine drug test dip card is a lateral flow chromatographic immunoassay for the detection of drugs and drug metabolites in human urine at following cut-off concentrations in urine:
The device is intended for the detection of drugs of abuse and/or metabolites in human urine for employment and insurance testing, or for forensic use screening purposes.
How to use
Test must be in room temperature (50.0℉ ~86.0℉/10 ºC ~30 ºC)
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Open the sealed pouch by tearing along the notch. Remove the test device from the pouch.
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Hold the one side of the device with one hand. Use the other hand to pull out the cap and expose the absorbent end.
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Immerse the absorbent end into the urine sample about 10 seconds. Make sure that the urine level is not above the “arrow” marker printed on the front of the device.
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Lay the device flat on a clean, dry, non-absorbent surface.
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Read the result at 5 minutes. Do not read 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.
Invalid
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.