// VITAMIN & SUPPLEMENT MANUFACTURING
Formulate to spec. Prove it by the lot.
Supplement manufacturing lives and dies on formulation accuracy, label dating, and traceability that holds up with retailers and auditors alike. Aurantium handles overages, retest dating, quality status, and recall readiness in one system.
The challenge.
Hitting label claim means building overages into the formula and proving potency by lot. Retest and expiration dates have to travel with the material and drive what ships. Big-box and online retailers expect EDI, advance ship notices, and compliant labels. Most ERPs make you bolt these on; Aurantium treats them as part of the core.
// HOW AURANTIUM FITS
From formula to retailer-ready pallet.
The details supplement manufacturers actually fight with, built in.
Per-component overages
Set an excess percentage on each formula line, so overages to hit label claim are part of the formula, not a side calculation.
Retest & expiration dating
Retest and expiration dates are first-class fields on every lot and drive FIFO shipment logic, so aging stock is caught before it ships.
Quality holds & release
Hold, quarantine, conditional-release and release states gate movement and shipping, with full history of every status change.
Lot genealogy & recall readiness
Lot-to-parent genealogy and a product where-used index turn a mock recall into a query instead of a week of digging.
Retailer EDI & ASN
Built-in EDI for purchase orders, advance ship notices, and invoices (850 / 856 / 810) with GS1 SSCC-18 pallet labeling.
Compliant labeling
A native ZPL label engine with barcodes and 2D codes prints lot, location, and shipment labels straight from live data.
// MORE INDUSTRIES
See it run a supplement batch.
Book a walkthrough and we'll take a sample product end to end: overage-built formula, lot dating, quality release, and a retailer-ready label.