Educational positioning
Artificial Excipient Free
No artificial flow agents or processing excipients in formula design.
Overview
Artificial excipient–free positioning targets formulation without synthetic flow agents or processing aids commonly flagged by clean-label buyers—while still meeting manufacturability requirements.
Typical documentation flow
High-level pathway Fieldston Wellness uses when aligning claims, suppliers, and buyer evidence—not a substitute for legal or regulatory advice for your jurisdiction.
Excipient inventory
Enumerate all processing aids across manufacturing steps.
Alternate engineering
Prototype blends with acceptable manufacturing windows.
Validation runs
Confirm QA outcomes without banned aids.
Claim packaging
Document definitions for retailer questionnaires.
Frequently asked questions
What counts as an excipient?
Typical examples include certain lubricants, glidants, or coatings. Exact lists depend on buyer definitions and regional pharmacopeia references.
Does removing excipients affect throughput?
It can. Feasibility studies balance clean-label goals with tablet hardness, fill weight, and line speed.
Further reading & related services
Internal workflows plus external references for deeper research. Links open in a new tab when they leave this site.
Apply this to your SKU mix
Talk to Fieldston Wellness about sourcing, documentation, and export-ready packs aligned to your certification story.