Bulk IngredientGanoderma lucidum
Reishi Mushroom Extract Powder
Fruiting-body extract for ingredient, formulation and private-label projects.
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REISHI INGREDIENT PARTNER
From cultivation in Guan County to batch-documented ingredients, finished formats and custom packaging.
CORE PORTFOLIO
Each project begins with species, part used, format, destination market and the documentation your team needs to evaluate the material.
Bulk IngredientGanoderma lucidum
Fruiting-body extract for ingredient, formulation and private-label projects.
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Bulk IngredientGanoderma lucidum spore powder
Sporoderm-broken powder with batch documentation and commercial packaging options.
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Finished FormatGanoderma lucidum spore oil
Private-label softgel projects with formula, shell and packaging coordination.
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Bulk IngredientGanoderma lucidum fruiting body
Dried fruiting-body slices for qualified botanical and herbal-product buyers.
View product brief →FARM TO COMMERCIAL BATCH
We structure the commercial conversation around identity, specification, sample evaluation and documented production.
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QUALITY COMMUNICATION
Qualified buyers can request the applicable specification, batch COA, testing scope, origin information and manufacturing documentation. Certificate names and claims are only used after their scope and current validity are confirmed.
VERIFIED CREDENTIALS
Current licenses and system certificates are separated from enterprise honors and destination-market approvals.
Organic production certificate
Certificate No. P77OP2500027 · valid through 27 July 2026
Red Reishi (Ganoderma lucidum), 60 tonnes, and Reishi spore powder, 36 tonnes; certified production area 5.333 hectares for each listed product.
Food-safety system
Valid through 3 November 2027
Specified production routes for broken cell-wall Reishi spore powder and capsules, plus entrusted production of Reishi spore-oil softgels.
Domestic production license
Valid through 24 July 2028
Licensed categories shown on the document include tea and related products and health foods.
Corporate recognition
Document details confirmed during qualification
A corporate technology recognition supporting company capability review.
PRIVATE LABEL & OEM
Move from requirement review to sample, label coordination, pilot order and documented production without mixing raw-material and finished-product responsibilities.
Explore the OEM workflow →Match part used, format and specification to the project.
Review powder, capsule, softgel, granule and blend routes.
Coordinate commercial pack options and buyer-provided market requirements.
Use approved samples and documents as the baseline for the pilot batch.