Official SodaSlim® distribution channel · authorized 2026 cycle · United States
SodaSlim®2026 authorized portal
Quality

SodaSlim Lab Standards: What Gets Tested on Every Lot

Every SodaSlim production run passes two gates before a single bottle ships: release testing inside the cGMP facility, then an independent file from Verimont Testing Laboratories, Inc.. This page describes the regimen; the result for the current run sits on the batch records page.

The facility

SodaSlim is manufactured in the United States in an FDA-registered facility operating under current Good Manufacturing Practices (cGMP). Registration does not mean the FDA approves the product - no supplement gets that - but it does mean the site is on the agency's inspection roster and runs documented procedures for cleaning, calibration, blend uniformity, and lot traceability. Every batch record starts there, with raw-material quarantine and weigh-room logs, before anything reaches an encapsulator.

The independent laboratory

Finished lots are sampled and couriered to Verimont Testing Laboratories, Inc., accredited to ISO/IEC 17025, the standard that governs testing-laboratory competence. Verimont holds no commercial stake in the product; its job is to say what is in the capsule, at what level, and whether contaminants sit below limits. The current certificate (VTL-4471-26) is referenced on the verification page and available to any buyer with an order number.

The per-lot battery

Tests run on every SodaSlim lot
TestMethodWhat it answers
Identity fingerprintHPLCAre the labeled botanicals actually the labeled botanicals?
Active assayHPLC-PDADoes active content meet specification? Current lot: 99.3%
Heavy metalsICP-MSLead, arsenic, cadmium, mercury below 0.4 ppm
Microbial limitsUSP <61> / <62>Total counts within limits; specified organisms absent
Pesticide screenGC-MS/MS panelBotanical inputs clear of residue above tolerance

Where the ingredients come from

Botanical inputs are bought against written identity specifications, not spot prices alone. Green tea and green coffee extracts arrive with supplier chromatograms that the facility re-verifies at intake; garcinia is purchased as standardized rind extract; caffeine anhydrous and raspberry ketone come from audited supplement-grade producers. A supplier that fails an intake fingerprint twice is removed from the approved list - the boring kind of rule that keeps a five-active label honest, since an undisclosed-ratio blend (see the composition review) is only as trustworthy as its inputs.

Format and allergen posture

The capsule shell is vegetarian, and the finished product is positioned by the maker as dairy-free and naturally gluten-free. No animal-derived actives appear on the label. Buyers managing specific allergies should read the printed panel on the physical bottle, which lists inactive ingredients for the exact run in hand.

Process here, result there. This page is the standing regimen; it changes rarely. The batch records page is the live result for the lot currently shipping, and it changes with every cycle. Read them as a pair.

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