Drug of Abuse (DOA)

Alcohol (ALC) Rapid Test

Detects Alcohol (ethanol). colloidal-gold. Specimen: Urine.

Alcohol (ALC) Rapid Test rapid diagnostic test — Progene Bio
Target / AnalyteAlcohol (ethanol)
Disease / IndicationDrug of abuse screening
SeriesDrug of Abuse (DOA)
Methodcolloidal-gold
SpecimenUrine
Test time10–15 min (product-specific)
Storage2–30 °C, sealed pouch with desiccant
Shelf life24 months (product-specific)
RegulatoryNon-CE / registration in progress
OEM/ODMAvailable — private label & custom panel

Direct Answer

This rapid test detects Alcohol (ethanol) in Urine to support Drug of abuse screening. It is a colloidal-gold screening test — a reactive result is presumptive and should be confirmed per the intended use.

Intended Use

Qualitative detection of Alcohol (ethanol) in urine for drug screening.

Clinical Context

Alcohol testing supports workplace and clinical screening. Cut-off typically 0.02%.

Test Principle

Colloidal-gold immunochromatography (lateral flow). The device captures the target analyte (antigen or antibody) on a membrane via labeled antibodies, producing a visible test line within minutes. Qualitative or semi-quantitative, intended as a screening/triage aid — not a replacement for confirmatory laboratory testing.

Limitations

Screening result — a presumptive positive requires confirmatory testing (GC-MS/LC-MS).

Procurement

Specimen: urine. Format: cassette / dipstick / panel. CE-marked line.

Interpretation

ResultLinesMeaning
PositiveTest + control lineTarget detected (presumptive positive)
NegativeControl line onlyBelow cut-off / not detected
InvalidNo control lineRepeat with a new device

Common misconception

A reactive drug-screen result is presumptive — it does not indicate impairment, timing of use or a diagnosis. Confirm positives by GC-MS/LC-MS.

Sources

Screening results are presumptive, not diagnostic. Confirmatory testing follows WHO, CDC and national regulatory guidance — see screening vs confirmatory.

Available SKUs (this series)

Cat. No.ProductSpecimenFormatKit SizeStatus
DAL-102 Alcohol (ALC) Rapid Test Cassette Urine Cassette 40 T CE
DAL-114 Alcohol (ALC) Rapid Test Panel Urine Panel 40 T CE
DAL-101 Alcohol (ALC) Rapid Test Dipstick Urine Dipstick 50 T CE
DAL-801 Alcohol Rapid Test Dipstick Oral Fluid Dipstick 50 T CE
DAL-802 Alcohol Rapid Test Cassette Oral Fluid Cassette 25 T CE
DAL-902 Breath Alcohol Test(With/Without Blow bag) Breath Cassette 15T/20 T CE

Technical Evidence

Analytical performanceSensitivity, specificity, cut-off and precision are documented per product line in the datasheet and validation report.
Average accuracy≥96% (overall agreement rate, manufacturer-validated). Per-product sensitivity and specificity are documented in the datasheet.
Clinical performanceEvaluation data (study population, reference method, agreement) available on request.
Cross-reactivityDocumented per analyte — see limitations above.
DocumentsIFU · Datasheet · Certificate · Declaration of Conformity — request below.

Buyer Information

MOQProduct-dependent — low MOQ available on specialty assays
OEM / private labelCustom branding, cut-off, panel and packaging
SamplesAvailable for evaluation — request via RFQ
Lead timeOn request
DocumentsIFU · Datasheet · COA · Validation report · CE files · Registration support

Documentation & quotation — datasheet, IFU, certificate, MOQ and OEM/ODM options on request.

Request IFU / Spec Sheet Request Datasheet Request Certificate

Last reviewed: 2026-09-12