CShybrid

Charlotte's Soda

Top flavors

earthyspicyfloral
CalmingEnergizing

Charlotte's Soda effects are mostly calming.

Charlotte’s Soda is a modern hybrid whose precise genetic origins remain undocumented and incomplete. While it is known to descend from Harle-Tsu, the remainder of its lineage consists of unnamed or undocumented parents, and no official breeder history has been publicly attributed to the strain. Due to these obscure origins, the development process and the initial intent behind its crossbreeding remain a mystery, marking it as a strain defined more by its physical traits and chemical output than by a recorded ancestral narrative.

This strain features a remarkably dense terpene profile that likely follows a specific order of expression, beginning with myrcene as the primary component, followed by secondary caryophyllene, linalool, limonene, and ocimene, with tertiary influences from humulene, pinene, nerolidol, beta-pinene, bisabolol, guaiol, and p-cymene. Its aroma and flavor profile tends to reflect the complexity of this heavy chemical loading, which likely contributes to a sophisticated sensory experience. Cultivation typically requires moderate skill when grown in either indoor or outdoor environments, yielding high results within a consistent 60-day flowering period.

As a THC-dominant cultivar, Charlotte’s Soda is formulated to induce effects that are consistently relaxed, happy, and uplifted. These characteristics make it a functional choice for users seeking support for stress, pain, or difficulties with sleep. While it serves as a distinct modern hybrid in the current market, there are currently no notable offspring recorded in its genetic lineage.

Terpene Profile

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

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

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.

~12%

floral

●●○○

Russo 2011: local anesthetic equal to procaine; anticonvulsant via glutamate/GABA modulation; reduces morphine tolerance via multisite opioid/GABAergic/cannabinoid action.

Effects

Reported effects — derived from terpene chemistry and cannabinoid profile.

Genetic Profile

Balanced Hybrid

■ Indica 50%■ Sativa 50%

Equal indica and sativa genetics. Balanced body and mind effects.

CBD-Dominant

High CBD, low THC. Non-intoxicating. Anti-inflammatory, anxiolytic, neuroprotective.

Genealogy

Parentage, ancestry, and genetic relatives of Charlotte's Soda.

Ancestry

Charlotte's SodaFull tree →
View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Charlotte's Soda

No verified dispensaries on file — find it on Leafly.

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What would Charlotte's Soda × ? 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 Charlotte's Soda

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Charlotte's Soda indica or sativa?

Charlotte's Soda is modeled here as a balanced hybrid (equal indica and sativa genetics).

What terpene is dominant in Charlotte's Soda?

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

Is Charlotte's Soda good for daytime use?

Charlotte's Soda 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.