PXhybrid-sativa
Hybrid-SativaModernTHC-Dominantmorning

Painkiller XL

9%

THC

0.3%

CBD

0.25%

CBG

Top flavors

earthypinespicy
CalmingEnergizing

Painkiller XL effects are mostly calming.

Low THCHigh THC

Painkiller XL is lower THC than average.

Painkiller XL is a modern hybrid-sativa cultivar bred directly from Royal Highness. Developed for its specific chemical composition, this strain balances its genetic architecture to prioritize a unique cannabinoid profile. It reaches harvest readiness in a 56-day flowering period, consistently providing high yields for growers operating in both indoor and outdoor environments. While cultivation requires a moderate skill level, the strain remains a reliable selection for those seeking professional-grade performance and stable development.

The aromatic and flavor profile of Painkiller XL is defined by its dominant concentration of terpinolene, which provides the foundation for its sensory experience. This is further nuanced by the secondary presence of myrcene and rounded out by a tertiary finish of caryophyllene. Together, these compounds create a distinct chemical profile that appeals to those sensitive to subtle botanical shifts, ensuring a consistent user experience rooted in the provided terpene hierarchy.

The cannabinoid profile of Painkiller XL is THC-dominant, containing approximately 9% THC alongside 0.3% CBD and 0.25% CBG. Users report that these levels produce effects characterized by creativity, uplifted mood, and happiness. Consequently, the strain is well-suited for activities requiring enhanced creativity, social engagement, or sustained focus. Currently, there is no recorded lineage of offspring derived from this cultivar, positioning it as a distinct end-point in its specific breeding line.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

myrcene ~60%pinene ~28%caryophyllene ~12%
TerpeneShare
myrcene~60%
pinene~28%
caryophyllene~12%

Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.

~60%

earthy

●●●○

Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.

~28%

pine

●●○○

Russo 2011: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.

~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.

Genetic Profile

Sativa-dominant

■ Indica 30%■ Sativa 70%

Primarily sativa with indica grounding. Uplifting with body relaxation.

THC-Dominant

High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.

Genealogy

Parentage, ancestry, and genetic relatives of Painkiller XL.

Composite Traits

Use caution if

sleep-seekingevening-wind-downpain-reliefdaytime-productivity

Where to buy Painkiller XL

No verified dispensaries on file — find it on Leafly.

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What would Painkiller XL × ? 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 Painkiller XL

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Painkiller XL indica or sativa?

Painkiller XL is modeled here as a sativa-dominant (primarily sativa with indica grounding).

What terpene is dominant in Painkiller XL?

Myrcene is shown as the dominant terpene at approximately ~60%. Pinene follows as the secondary terpene.

Is Painkiller XL good for daytime use?

Painkiller XL 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.