ToxTilt Urine Drug Test Cup

Tilt-Activated Collection Design:

Enables quick and efficient test activation with a simple tilt mechanism.

Integrated Temperature Validation:

The ToxTilt Urine Drug Test Cup has an inbuilt temperature strip that lets you monitor the temperature of the urine sample so you can ensure that the sample hasn’t been tampered with.

Spill-Reducing Construction:

Secure cup construction helps minimise spills and improve handling during testing procedures.

Adulterant Integrity Screening:

The kit also includes six adulterant test strips that can detect adulterants such as pH, nitrite, oxidants, specific gravity, creatinine, and glutaraldehyde.

Streamlined Workplace Testing:

Includes urine collection cup, integrated test strips, adulterant checks, and adulterant colour chart for streamlined testing.

Drugs Detected

Cannabis/THC (THC) Methamphetamines (MET) Cocaine (COC) Amphetamines (AMP) Benzodiazepines (BZO) Opiates (OPI)

Cut-Off Levels

Cannabis/THC (THC): 50 ng/mL Methamphetamines (MET): 300 ng/mL Cocaine (COC): 150 ng/mL Amphetamines (AMP): 300 ng/mL Benzodiazepines (BZO): 200 ng/mL Opiates (OPI): 300 ng/mL

Units per Box

25

Sample Type

Urine

Adulterants Detected

Creatinine Specific Gravity pH Oxidants Nitrite Glutaraldehyde

Temperature Strip

Yes

Dimensions:

8.7 x 7.7 x 7.7 cm

Weight:

37 grams

1. Pre-Testing Hydration Requirements

Donors must maintain normal hydration but restrict water intake to a maximum of 500 mL in the hour before testing to prevent a diluted sample.

2. Collect the Sample

Have the donor provide a urine sample directly into the collection cup. Ensure the urine level is above the minimum volume line (typically around 30 mL) to guarantee there is a sufficient amount of specimen for both the initial testing and any potential laboratory confirmation if required.

3. Verify Sample Temperature

Immediately check the built-in temperature strip on the cup. To verify the sample has not been substituted or tampered with, the green indicator should show a temperature between 32°C and 38°C within 4 minutes of collection.

4. Secure the Lid

Firmly screw the lid onto the cup until it is fully sealed. Ensuring a tight, secure seal is critical for hygienic purposes.

5. Prepare for Activation

Place the sealed cup upright on a clean, flat, horizontal surface.

6. Activate the Test (Tilt the Cup)

Tilt the cup completely onto its side, resting it securely on its raised flat edge. This specific tilting action activates the test by allowing the collected specimen to flow out of the main chamber and directly into the channels containing the test strips.

7. Set the Timer

Immediately start a timer for 5 minutes after activation. Allow the cup to sit undisturbed on the flat surface while the results develop.

8. Read Adulteration Results (3–5 Minutes)

Using the integrated adulteration/validity test strips, read these results between 3 and 5 minutes after tilting. Compare the strip colors to the included color reference chart to verify the integrity and validity of the specimen.

9. Interpreting Negative Results

Look at the Control (C) and Test (T) regions for each drug strip. A Negative result is indicated when a colored line appears next to both the Control (C) and the Test (T) region.

10. Interpreting Preliminary Positive Results

A preliminary positive result is indicated when a colored line appears next to the Control (C) region, but no line appears next to the Test (T) region. This indicates the presumptive presence of the target drug or metabolite.

11. Identify Invalid Results & Observe Time Limits

An Invalid result occurs if no line appears next to the Control (C) region, regardless of whether a line shows up in the Test (T) region. If a strip is invalid, the test is void and you must repeat the entire procedure using a brand-new cup and a new sample.