LSOhybrid-indica
Hybrid-IndicaModernTHC-Dominantafternoon

Lemon S.A.G.E. OG

Top flavors

spicyearthycitrus
CalmingEnergizing

Lemon S.A.G.E. OG has balanced effects.

Lemon S.A.G.E. OG is a modern hybrid-indica variety developed from a genetic cross between an unknown strain and Foo Dog. As a result of this pairing, its lineage remains partly undocumented, blending the traits of a mystery cultivar with established genetics to create a distinct profile. The strain is well-regarded for its adaptability, performing reliably in both indoor and outdoor environments. Growers can expect a high yield from this moderate-difficulty plant, which reaches maturity after a 63-day flowering period.

The chemical complexity of Lemon S.A.G.E. OG is defined by its extensive terpene profile, which is led by a dominant presence of caryophyllene followed by myrcene and limonene. Secondary and tertiary contributions from pinene, humulene, and ocimene provide subtle nuance, while the inclusion of nerolidol, linalool, beta-pinene, guaiol, p-cymene, bisabolol, eucalyptol, camphene, and caryophyllene-oxide rounds out the specimen’s organoleptic composition. This blend results in a sophisticated sensory experience that captures the underlying chemistry of its diverse lineage.

This THC-dominant hybrid is primarily noted for inducing a relaxed, calm, and focused physical and mental state. These characteristics make the strain a functional choice for those seeking to manage symptoms of pain, stress, or issues related to sleep. Beyond its immediate effects on the user, the plant has left a mark on modern breeding as the parent of its notable offspring, Droppin Dat Ass.

Terpene Profile

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

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

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.

~28%

earthy

●●●○

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

~12%

citrus

●●○○

Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.

Effects

Reported effects — derived from terpene chemistry and cannabinoid profile.

Genetic Profile

Indica-dominant

■ Indica 70%■ Sativa 30%

Primarily indica with sativa influence. Relaxing body with some cerebral lift.

THC-Dominant

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

Genealogy

Parentage, ancestry, and genetic relatives of Lemon S.A.G.E. OG.

Offspring — 1 strains bred from Lemon S.A.G.E. OG

View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Lemon S.A.G.E. OG

No verified dispensaries on file — find it on Leafly.

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What would Lemon S.A.G.E. OG × ? 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 Lemon S.A.G.E. OG

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Lemon S.A.G.E. OG indica or sativa?

Lemon S.A.G.E. OG is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in Lemon S.A.G.E. OG?

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

Is Lemon S.A.G.E. OG good for daytime use?

Lemon S.A.G.E. OG 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.