After ingestion, symptoms such as drowsiness, dizziness, loss of balance, and memory impairment can appear within 15–30 minutes, and the effects may last for 3–6 hours.
When combined with alcohol, the risks are even more severe,
potentially causing respiratory depression, loss of consciousness, and other life-threatening effects.
GHB, also known as “liquid ecstasy” or a “date rape drug,”
is a central nervous system depressant.
It is nearly colorless, odorless, and tasteless, making it difficult for victims to detect when mixed into alcoholic drinks or beverages.
Because of this, it is often misused in crimes.
“ In recent years, related crimes have been increasing both domestically and internationally.”
GHB Drug Test Sticker
Angel Guard – ShineB
The World’s First Nail Art-Type GHB Detection Sticker
Simple Test with Just One Drop of a Drink
Providing Both Portability and Fashion
“ Naturally wearable in any situation…”
If GHB is detected, half of the sticker changes to green
Note: This product is for one-time use only. For testing another drink, please use a new sticker.
* Conventional Products
* AngelGuard:
With the motto “Health is the basis of beauty”, SHINE B is putting more effort into improving product quality and stability to remove the preconceived notion that the nail art products are chemical..
Production Manufacturing after Selecting the Manufacturing Method in Consideration of the Difference Between Offset Printing and Screen Printing
A01 : This product does not fall under medical devices, diagnostic tools, or cosmetics. It is classified as a general consumer safety product.
–AngelGuard is a preventive safety support tool for consumer protection.
–It has no purpose of medical diagnosis or treatment related to disease, crime, or safety checks.
A02 : No. AngelGuard is not classified as a “Home-use diagnostic test kit”
–Therefore, FDA regulations for medical devices (IVD) do not apply.
–AngelGuard is not intended for medical diagnosis or legal proof, but is classified as a safety consumer product or preventive support tool.
–Compliance with local regulations must be verified and ensured by local importers and distributors.
A03 : A home-use diagnostic test kit is a medical device that allows consumers to check diseases or health conditions at home.
Examples: COVID-19 rapid antigen test kits, pregnancy test kits, blood glucose or cholesterol self-test kits.
These products are classified as In Vitro Diagnostic Devices (IVD) and must be approved by the FDA before sale.
A04 : An IVD is a medical device that uses human samples (blood, saliva, urine, etc.) to diagnose, detect, or monitor disease, infection, or health conditions outside the human body.
In the U.S., IVDs are regulated as medical devices, and FDA reviews their safety, performance, and accuracy.
They generally require 510(k) submission, De Novo pathway, or PMA (Pre-Market Approval) before entering the market.
In short, IVDs have diagnostic and medical effectiveness, whereas AngelGuard is fundamentally different.
A05 : FDA Registration: AngelGuard is not a medical device, so it is not subject to FDA registration.
ISO Certification: The production process can be managed under ISO quality standards (e.g., ISO 9001).
However, the product itself is not subject to medical device ISO certification (e.g., ISO 13485).
A06 : AngelGuard is not intended for medical diagnosis or treatment.
Test results are for reference only and serve as a preventive safety tool, not a 100% guaranteed solution.
Responsibility for interpretation and usage lies with the end user.
The company does not bear any legal liability for incidents arising from the use of this product.
A07 : No. AngelGuard was specifically developed to detect GHB (γ-Hydroxybutyrate).
It does not guarantee detection performance for other narcotics or chemical substances.
A08 : Yes, it is possible.
The color change relies on visual interpretation, so results may vary depending on lighting, drink color, and the user’s perception.
Therefore, results should not be used as sole evidence, but rather as a supportive safety tool.
A09 : AngelGuard is a consumer safety product designed for preventive support.
The company does not take responsibility for direct/indirect damages, legal disputes, or criminal incidents resulting from product use.
Compliance with national import regulations and distribution requirements lies with the importer/distributor.
A10 : –Storage: Avoid direct sunlight, high temperature, and humidity.
–Shelf life: Accuracy may decrease after 36 months from manufacturing date.
–Usage: Lightly touch the test area to the beverage → check for color change within the indicated time.
–Caution: Strongly colored drinks or high-proof alcohol may affect interpretation.
–Time limit: Do not interpret results after 5 minutes, as the color may shift to a false positive.
–Single-use product: For new tests, always use a new sticker.
–Application: The product can be attached to nails or simple surfaces, but misuse may reduce sensitivity and cause false positives.
→ Recommended to apply 1–2 hours before use for best performance.
A11 : OEM/ODM customization is possible if the minimum order quantity (MOQ) set by the company is met.
Basic principles: Packaging type, size, and test quantity defined by the company must be maintained,
Packaging design can be fully adapted to customer branding.
Product design (size, shape, color) can be customized to a certain extent, though limitations may apply
A12 : Yes, the key performance has been verified through internal testing.
– Filmedi Internal Analytical Performance Test results:
· Sensitivity (LoD, Limit of Detection): Detectable at 1% (10 mg/mL) GHB
· Specificity (Cross-reactivity/Interference tests): Normal responses confirmed in most beverages
This is a common limitation across all products and should be disclosed transparently.
② Red wine, cola, coffee and other dark-colored drinks → Normal reactions occur, but strong coloration may cause visual confusion during result interpretation.
Therefore, the possibility of visual misinterpretation must be clearly communicated.
– External testing: Performance test requested to a U.S. professional institute (Company M), with final report expected in Oct–Nov 2025.
– Conclusion: This product is a preventive safety support tool against drink spiking crimes and not a 100% definitive diagnostic device, which must be clearly stated.
A13 : It refers to an internationally recognized risk threshold.
– Based on an average adult female (50 kg body weight), if approximately 1% GHB is mixed into one glass of beverage, it is defined as the minimum level that
affects physical and mental functions.
– In other words, it represents the minimum concentration at which criminal attempts become feasible.
Any concentration above this must be detectable according to international standards.
– AngelGuard is capable of detection even at 0.1% concentration, confirming much higher sensitivity than the general standard.
This means the product demonstrates 10 times greater sensitivity compared to the global benchmark.
Please don’t hesitate to contact us for any details you are interested in. Our agents will gladly answer any of your questions.