Numbing Effect
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Terpenes
Numbing Effect effects are mostly calming.
Numbing Effect
Numbing Effect is a modern hybrid strain derived from the genetic lineage of Legend Orange Apricot. Designed for consistent production, this strain features a moderate cultivation difficulty and thrives in both indoor and outdoor environments. Growers can expect a high yield from this variety, which reaches maturity following a 63-day flowering cycle. Its genetic utility is further verified by its use as a parent in breeding programs, most notably in the cross of Numbing Effect and Black Lime Reserve.
The chemical profile of Numbing Effect is dominated by myrcene, followed by limonene, caryophyllene, and linalool. The secondary and tertiary terpene structure rounds out with humulene, beta-pinene, pinene, bisabolol, terpinolene, borneol, valencene, nerolidol, camphene, geraniol, and caryophyllene-oxide. This complex array informs the sensory experience, balancing the earthy foundations of myrcene against the bright, citrus-forward notes derived from the limonene content.
As a THC-dominant cultivar, Numbing Effect is primarily associated with feelings of being relaxed, happy, and uplifted. These therapeutic properties make it a frequent selection for the management of stress, pain, and sleep difficulties. Given its capacity to promote physical and mental ease, the strain maintains a functional role in the modern cannabis landscape, serving both as a direct utility for end users and a foundational genetic component for future breeding projects.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| limonene | ~28% | citrus | social · creative |
| caryophyllene | ~12% | spicy | relaxing · social |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
~12%
spicy
●●○○
Russo 2011: only terpene that is a selective full CB2 agonist (100 nM); Gertsch et al. 2008: acts as dietary cannabinoid; unique anti-inflammatory and gastric cytoprotective properties.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
happy
anytimeuplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Balanced Hybrid
Equal indica and sativa genetics. Balanced body and mind effects.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Numbing Effect.
Composite Traits
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What would Numbing Effect × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
Build a cross with Numbing Effect →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Numbing Effect indica or sativa?
Numbing Effect is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Numbing Effect?
Myrcene is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.
Is Numbing Effect good for daytime use?
Numbing Effect is versatile and works across different times of day depending on dose and individual response.
How accurate is this data?
See the "Data confidence" card in the sidebar. Terpene profiles and effects are chemistry-informed estimates — individual responses depend on phenotype, source, and personal chemistry.