Healstone Accurate® 15 Panel Urine EZ Split Drug Test Cup 25/Box
Brand : Healgen Scientific
$129.00
- Per Each:
- 25
Healstone Accurate® Drugs of Abuse 15 Panel EZ Split Drug Test Cup by Healgen Scientific
Self Contained Split Specimen Urine Drug Testing
The Healstone Accurate® from Healgen Scientific is a comprehensive urine test cup that simultaneously screens for qualitative detection of up to 15 drugs of abuse in minutes. Featuring a dual specimen chamber, the Accurate™ Drug of Abuse Urine EZ Split Cup securely channels urine specimen into separate reservoirs for initial screening and retention.
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Benefits
- FDA 510(k) Cleared for Over-the-Counter use
- CLIA Waived
- 24 Month Shelf Life from Date of Manufacture
- Simultaneously Test for Up to 15 Drugs
- On-site Drug Screening
- Split Specimen Testing
- Qualitative Results in 5 Minutes
- Operator Controlled Test Activation
- Specimen Temperature Indication
- Integrated Specimen Validity Tests to Detect Urine Adulteration
Features | |
 | Leak Resistant Lid Large, Angled Opening |
 | Dual Specimen Chamber Residual Sample Testing |
 | Rotating Key On demand test activation is triggered by turning unidirectional base. |
 | Multiplex Testing Sample-Free Result Window Flat Result Window |
Download and Print Product Documentation
Drugs of Abuse Urine EZ Split Cup Package Insert
| 15 Panel Configurations (Choose Above) | ||
| Item Number | Drugs Tested | Approvals |
| HCDOACI-2145S | AMP500, BAR300, BUP10, BZO300, COC150, EDDP300, MDMA500, MET500, MTD300, OPI2000, OXY100, PCP25, PPX300, TCA1000, THC50 | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| HCDOACI-2155 | AMP500, BAR300, BUP10, BZO300, COC150, EDDP300, MDMA500, MET500, MOP300, MTD300, OXY100, PCP25, PPX300, TCA1000, THC50 | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Drug Detection Table in Urine | ||||
| Drug Name | Abbreviation | Cutoff | Detection Times * | Certifications |
| Amphetamines - Amphetamine and the structurally related “designer” drugs are sympathomimetic amines whose biological effects include potent central nervous system (CNS) stimulation, anorectic, hyperthermic, and cardiovascular properties. They are usually taken orally, intravenously, or by smoking. Amphetamines are readily absorbed from the gastrointestinal tract and are then either deactivated by the liver or excreted unchanged in the urine with a half-life of about 12 hours. It can be detected in the urine for 1 to 2 days after use. Amphetamine is metabolized to deaminated (hippuric and benzoic acids) and hydroxylated metabolites. Methamphetamine is partially metabolized to amphetamine and its major active metabolite. Amphetamines increase the heart rate and blood pressure and suppress the appetite. Some studies indicate that heavy abuse may result in permanent damage to certain essential nerve structural in the brain. | AMP | 500 or 1000 ng/mL | 2 hours to 4 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Barbiturates - Barbiturates are a class of central nervous system depressions. They have a wide range of half-life of 2 to 40 hours and can be detected in the urine for 1 to 4 days after use. Phenobarbital is a long-acting barbiturate derivative that has been used as a daytime sedative and very extensively as an anticonvulsant. Pentobarbital and secobarbital are two examples of a short-acting barbiturate sedative. Abuse of barbiturates can lead not only to impaired motor coordination and mental disorder but also to respiratory collapse, coma, and even death. Barbiturates are taken orally, rectally, or by intravenous and intramuscular injections. Short-acting barbiturates will generally be excreted in urine as metabolites, while the long-acting barbiturates will primarily appear unchanged. | BAR | 300 ng/ml | 2 hours to 3 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Benzodiazepines - Benzodiazepines are medications that are frequently prescribed for the symptomatic treatment of anxiety and sleep disorders. They produce their effects via specific receptors involving a neurochemical called gamma-aminobutyric acid (GABA). Because they are safer and more effective, Benzodiazepines have replaced barbiturates in the treatment of both anxiety and insomnia. Benzodiazepines are also used as sedatives before some surgical and medical procedures, and for the treatment of seizure disorders and alcohol withdrawal. | BZO | 300 ng/ml | 2 hours to 4 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Buprenorhine / Suboxone - Buprenorphine is a semi-synthetic opioid derived from thebaine, an alkaloid of the poppy Papaver somniferum. Buprenorphine is an opioid partial agonist. This means that, although Buprenorphine is an opioid, and thus can produce typical opioid effects and side effects such as euphoria and respiratory depression, its maximal effects are less than those of full agonists like heroin and methadone. At low doses Buprenorphine produces sufficient agonist effect to enable opioid-addicted individuals to discontinue the misuse of opioids without experiencing withdrawal symptoms. The agonist effects of Buprenorphine increase linearly with increasing doses of the drug until it reaches a plateau and no longer continues to increase with further increases in dosage. This is called the "ceiling effect." Thus, Buprenorphine carries a lower risk of abuse, addiction, and side effects compared to full opioid agonists. In fact, Buprenorphine can actually block the effects of full opioid agonists and can precipitate withdrawal symptoms if administered to an opioid-addicted individual while a full agonist is in the bloodstream. This is the result of the high affinity Buprenorphine has to the opioid receptors. The affinity refers to the strength of attraction and likelihood of a substance to bind with the opioid receptors. | BUP | 10 ng/ml | 2 hours to 3 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Cocaine - Cocaine derived from leaves of the coca plant, is a potent central nervous system stimulant and a local anesthetic. Among the psychological effects induced by using cocaine are euphoria, confidence and a sense of increased energy, accompanied by increased heart rate, dilation of the pupils, fever, tremors, and sweating. Cocaine is excreted in the urine primarily as benzoylecgonine in a short period of time. | COC | 150 or 300 ng/ml | 1 hour to 4 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Ecstasy - Methylenedioxymethamphetamine (ecstasy) is a designer drug first synthesized in 1914 by a German drug company for the treatment of obesity. Those who take the drug frequently report adverse effects, such as increased muscle tension and sweating. MDMA is not clearly a stimulant, although it has, in common with amphetamine drugs, a capacity to increase blood pressure and heart rate. MDMA does produce some perceptual changes in the form of increased sensitivity to light, difficulty in focusing, and blurred vision in some users. Its mechanism of action is thought to be via release of the neurotransmitter serotonin. MDMA may also release dopamine, although the general opinion is that this is a secondary effect of the drug (Nichols and Oberlender, 1990). The most pervasive effect of MDMA, occurring in virtually all people who took a reasonable dose of the drug, was to produce a clenching of the jaws. | MDMA | 500 ng/ml | 2 hours to 4 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Marijuana - Cannabinoid is a hallucinogenic agent derived from the flowering portion of the hemp plant. The active ingredients in Cannabinoids, THC & Cannabinol can be metabolized and excreted as 11-nor- Δ9-tetrahydrocannabinol-9carboxylic acid with a half-life of 24 hours. It can be detected for 1 to 5 days after use. Smoking is the primary method of the use of Cannabinoids/cannabis. Higher doses used by abusers produce central nervous system effects, altered mood and sensory perceptions, loss of coordination, impaired short-term memory, anxiety, paranoia, depression, confusion, hallucinations, and increased heart rate. A tolerance to the cardiac and psychotropic effects can occur, and withdrawal syndrome produces restlessness, insomnia, anorexia, and nausea. | THC | 50 ng/ml | 2 hours to 4 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Methadone - Methadone is a synthetic analgesic drug that is originally used in the treatment of narcotic addicts. Among the psychological effects induced by using methadone are analgesia, sedation, and respiratory depression. Overdose of methadone may cause coma or even death. It is administered orally or intravenously and is metabolized in the liver and excreted in urine as methadone, EDDP, EMDA, and methanol. The kinneys are a major route of methadone excretion. Methadone has a biological half-life of 15 to 60 hours. | MTD | 300 ng/ml | 3 hours to 3 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Methadone Metabolite - Test for the qualitative determination of EDDP (2-ethylidene-1,5-dimethyl-3,3- diphenylpyrrolidine) in human urine at a Cut-Off concentration of 300 ng/mL.The benefit of measuring EDDP instead of methadone is that individuals in methadone programs sometimes divert their methadone into the illicit drug market and then spike their urine sample with a small quantity of methadone to cover the diversion. Their urine sample may test positive for methadone but would not test positive for EDDP. | EDDP | 300 ng/ml | 1 hour to 3 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Methamphetamines - Methamphetamine is a potent sympathomimetic agent with therapeutic applications. Acute higher doses lead to enhanced stimulation of the central nervous system and induce euphoria, alertness, and a sense of increased energy and power. More acute responses produce anxiety, paranoia, psychotic behavior, and cardiac dysrhythmias. The pattern of psychosis which may appear at half-life of about 15 hours and is excreted in urine as amphetamine and oxidized as deaminated and hydroxylated derivatives. However, 40% of methamphetamine is excreted unchanged. Thus the presence of the parent compound in the urine indicates methamphetamine use. | mAMP | 500 or 1000 ng/ml | 2 hours to 4 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Morphine / Opiates - The opiates such as heroin, morphine, and codeine are derived from the resin of opium poppy. The principal metabolites of opiates are morphine, morphine-3-glucuronide normorphine, and codeine with a half-life of about 3 hours. Heroin is quickly metabolized to morphine. Thus, morphine and morphine glucuronide might both be found in the urine of a person who has taken only heroin. The body also changes codeine to morphine. Thus, the presence of morphine (or the metabolite, morphine glucuronide) in the urine indicates heroin, morphine and/or codeine use. The test for Morphine (MOP) of the Multi-Drug Urine Test Panel yields a positive result when the morphine in urine exceeds 300ng/mL. | MOP / OPI | 300 or 2000 ng/mL | 2 hours to 3 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Oxycodone - Oxycodone is known as Oxycontin and Roxicodone. It is an ingredient of Percodan, Percocet, Roxicet, and Tylox. Oxycodone is a semi-synthetic opiate derived from opium. Like other opiates, Oxycodone is characterized by its analgesic properties, and the tendency for users to form a physical dependency and develop tolerance with extended use. Oxycodone is usually administered in combination with non-opiate analgesics such as acetaminophen and salicylates for the relief of moderate to severe pain. Oxycodone is a central nervous system depressant that may cause drowsiness, dizziness, lethargy, weakness, and confusion. Toxicity in an overdose of Oxycodone can lead to stupor, coma, muscle flaccidity, severe respiratory depression, hypotension, and cardiac arrest. Oxycodone is metabolized by N- and O-demethylation. One of the metabolites, oxymorphone, is a potent narcotic analgesic, while the other, nor oxycodone, is relatively inactive. Between 33 to 61% of a single dose of Oxycodone is excreted in a 24-hour urine collection and consists of 13-19% free Oxycodone, 7-29% glucuronide conjugated Oxycodone, 13-14% glucuronide conjugated oxymorphone and an unknown amount of nor oxycodone. The detection time window of Oxycodone is 1-3 days following use. | OXY | 100 ng/ml | 1 hour to 2 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Phencyclidine - Phencyclidine is an arylcyclohexylamine that was originally used as an anesthetic agent and a veterinary tranquilzer. Phencyclidine can produce hallucinations, lethargy, disorientation, loss of coordination, trance-like ecstatic states, a sense of euphoria and visual distortions. It has many street names, such as “angel dust” and “crystal cyclone,” etc. phencyclidine can be administered orally, by nasal ingestion, smoking, or by intravenous injection. It is metabolized in the liver and excreted through the kidneys in urine in unchanged form and oxidized metabolites with a half life of about 12 hours. Suction and urinary acidification in the treatment of overdose typically reduces its half-life from three days to one day. | PCP | 25 ng/ml | 4 hours to 14 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Propoxyphene - This test will be positive if the sample tested contains at least 300 nanograms of propoxyphene or norpropoxyphene, Propoxyphene is a prescription drug for the relief of pain. Propoxyphene hydrochloride (Darvon, Dolene, and others) is available in 32mg and 65mg capsules; propoxyphene napsylate (Darvon-N) is available in 100mg tablets or as a suspension. It is structurally related to methadone. | PPX | 300 ng/ml | 1 hour to 3 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| Tricyclic Antidepressants / Nortriptyline - chemical compounds used primarily as antidepressants discovered in the early 1950s. The first TCA reported for the treatment of depression was imipramine used primarily in the clinical treatment of mood disorders such as major depressive disorder (MDD). Tricyclic antidepressants are possibly more effective in treating melancholic depression than other antidepressant drug classes. | TCA | 1000 ng/ml | 8 hours to 7 days | FDA 510(k) Cleared Over-the-Counter Use CLIA Waived |
| * Detection times are not guaranteed. This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas Chromatography/Mass Spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated. | ||||
