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Informational content; does not constitute legal advice. EUM class: raw material (input) for manufacturing the finished product. It is not a shelf product: it is a B2B input. EUM does not sell or handle CBD alone — the catalog is multi-cannabinoid.

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1. Classification

  • Input / raw material for manufacturing a finished product. It does NOT go to the end consumer → it does not carry NOM-051 seals or consumer labeling (those apply to the finished product that incorporates it — see Anatomy of a compliant label).
  • It carries an input identification label (not a shelf label) + its technical data sheet and COA.
Do not confuse the three: raw material (this class) ≠ finished product ≠ ingredient. The difference and the decision rule are in Label anatomy · the three regimes.

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Cannabinoids that EUM handles as raw material

It is not only CBD. The input can be any of these (natural or semisynthetic), always ≤1% THC:
THC isomers (Δ8, Δ10…) are NOT sold as raw material — they count as THC. Δ8 is covered by EUM’s amparo (it is considered much lighter than Δ9, which is the basis of the amparo), but is offered only in EUM finished products, within the ≤1% total-THC cap. To incorporate it into a product, the path is contract manufacturing / partnership with EUM, not buying the input.
Each input arrives with its COA per batch (Smart COA) and is linked to the COA of the finished product that incorporates it. The legal coverage by substance/category is summarized in Regulatory traceability.

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2. Procedure / regulatory basis

  • Framework ≤1% THC: Art. 245 sect. V LGS; hemp raw material for industrial uses operates under amparo coverage by class (internal case files that are presented to the authority when required).
  • Importation: hemp raw material ≤1% THC — free importation without prior sanitary permit (COFEPRIS criterion); see Importation and customs. Related: Ley Federal de Sanidad Vegetal (LFSV) (Federal Plant Health Law) for plant inputs.

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3. Input labeling (identification, not consumer)

The raw material carries an identification/handling label, not the consumer label (NOM-051). Its purpose is to identify the input and its batch for whoever transforms it, not to inform a shelf buyer:
  • Identification label: input denomination, identity and concentration/spectrum, batch, manufacturer/importer/distributor, storage/handling conditions and expiration — in accordance with Art. 25 RCSPS. The system generates this identification label (premium format) distinct from the simple label of the finished product.
  • Identification/handling framework: the communication of identity and handling of a chemical input relies on the NOM-018 framework (identification and communication of hazards/handling of substances). (The exact citation and its applicability to the input are confirmed with the legal team; it is documented as the framework the system targets, without overclaim.)
  • Technical data sheet (identity, concentration, spectrum) + COA per batch (the analysis is THE key document of the input) + certificate of origin/importation when applicable.
  • No NOM-051 seals, no nutrition table, no consumer denomination.
  • Batch traceability via Smart COA; when used in a finished product, its COA is linked to the product’s COA (see Smart COA · ingredient traceability).

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4. What the EUM system RESOLVES

  • COA per batch + traceability is exactly the core of the system (Smart COA) — the raw material is born with its analysis and is linked to the finished products that use it (total potency / shared COA).
  • Consumer labeling (seals, statements) is resolved in the finished product, not here.

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5. Sources

Last updated: 2026-08-01 · official sources cited above. Informational, does not constitute legal advice.