Quick Answer: Lymph Go is manufactured in FDA-registered facilities following current Good Manufacturing Practices (cGMP). Every batch undergoes rigorous testing for purity, potency, and safety before release. Third-party verification ensures our quality claims are accurate and verifiable.
In the dietary supplement industry, quality standards vary dramatically between manufacturers. Some companies prioritize low costs and high profits over quality, resulting in products that contain less than claimed amounts of active ingredients, include undisclosed fillers or contaminants, or are manufactured under questionable conditions.
Lymph Go takes a fundamentally different approach. We apply pharmaceutical-grade manufacturing standards to ensure every jar you receive meets the highest quality and safety specifications. This commitment to quality is non-negotiable—it's the foundation of everything we do.
Lymph Go is manufactured in facilities registered with the U.S. Food and Drug Administration (FDA). FDA registration is not merely a formality—it subjects facilities to FDA inspections and requires adherence to strict manufacturing and safety protocols.
What FDA Registration Means:
Current Good Manufacturing Practices (cGMP) represent the gold standard for supplement manufacturing. These comprehensive regulations, established by the FDA, cover every aspect of production to ensure consistent quality, purity, and safety.
Personnel Training and Qualification: All personnel involved in manufacturing must be appropriately trained and qualified for their roles. This includes understanding quality procedures, hygiene requirements, equipment operation, and documentation practices.
Facility Design and Maintenance: Manufacturing facilities must be designed to prevent contamination and mix-ups. This includes separate areas for different production stages, adequate lighting and ventilation, pest control systems, and regular equipment maintenance and calibration.
Equipment Standards: All equipment that contacts ingredients or finished product must be constructed of appropriate materials (typically stainless steel), cleaned and sanitized between batches, calibrated regularly to ensure accuracy, and maintained according to strict schedules.
Raw Material Controls: Every ingredient must be tested for identity and purity before use. Suppliers must be qualified and regularly audited. Certificates of Analysis must be obtained and reviewed. Materials must be stored properly to prevent degradation.
Production Process Controls: Manufacturing processes must be validated to ensure consistency. Critical control points must be monitored continuously. In-process testing must verify the product at key stages. Any deviations from standard procedures must be investigated.
Quality Control Testing: Finished products must be tested for identity, purity, potency, and composition. Microbiological testing ensures safety. Stability testing confirms shelf life. Products cannot be released until all specifications are met.
Documentation and Record Keeping: Comprehensive records must document every step from raw materials to finished product. Batch records track materials used, processing conditions, and test results. Records must be maintained for specified periods and available for audits.
Quality assurance begins before ingredients enter our manufacturing facility. Every raw material undergoes rigorous testing before being approved for use in Lymph Go.
We must confirm that each ingredient is exactly what it claims to be. This isn't as simple as it sounds—botanical materials can be easily confused or adulterated. We use multiple analytical techniques:
HPLC (High-Performance Liquid Chromatography): This sophisticated technique separates and identifies chemical compounds in plant materials. Each botanical has a unique chemical "fingerprint" that HPLC reveals. We compare this fingerprint to reference standards to confirm identity.
Mass Spectrometry: This technique determines the molecular weight and structure of compounds in materials. It provides definitive identification of specific substances.
Microscopic Analysis: For botanical materials, trained botanists examine samples under microscopy to confirm species identification based on cellular structures.
Beyond confirming identity, we must ensure ingredients are pure and free from contaminants:
Heavy Metals Testing: We test for lead, cadmium, mercury, and arsenic—toxic metals that can contaminate botanical materials from soil or water. Our specifications are more stringent than regulatory requirements.
Pesticide Screening: Multi-residue pesticide testing screens for hundreds of agricultural chemicals. Only materials meeting strict purity standards are accepted.
Microbiological Testing: We test for harmful bacteria (E. coli, Salmonella), yeast, mold, and other microorganisms. Materials must meet pharmaceutical-grade specifications for microbiological purity.
Solvent Residue Analysis: Some extraction processes use solvents. We verify that any residual solvents are below safe limits established by health authorities.
Active ingredients must be present at specified levels. Using analytical techniques like HPLC and UV spectroscopy, we quantify active compounds to ensure potency meets specifications. Materials with inadequate potency are rejected.
During manufacturing, we monitor critical control points to ensure the product is developing correctly:
Weighing Verification: Ingredients are weighed using calibrated scales with accuracy verified. Two independent personnel confirm weights match specifications.
Mixing Homogeneity: Samples taken from different locations in the mixer are analyzed to ensure uniform distribution of all ingredients. This ensures every scoop contains the same amount of each ingredient.
Moisture Content: Powders must have specific moisture levels. Too much moisture promotes microbial growth; too little makes powder handling difficult. Moisture is measured and adjusted as needed.
Particle Size: The powder must have appropriate particle size for good mixing characteristics and dissolution. We use laser diffraction to measure particle size distribution.
Environmental Monitoring: Temperature, humidity, and air quality in production areas are continuously monitored to ensure conditions remain within specifications.
Before any batch is released for sale, comprehensive testing confirms it meets all quality specifications:
We verify the finished product contains all eight ingredients at appropriate levels using HPLC and other analytical methods.
Active compounds are quantified to confirm they match label claims. Acceptable ranges are typically 90-110% of label claim, though we aim for even tighter control.
Finished product undergoes the same rigorous microbiological testing as raw materials. This includes total aerobic plate count, yeast and mold counts, absence of pathogens (E. coli, Salmonella, Staphylococcus aureus), and absence of coliforms.
Even though ingredients are tested, finished product is also screened for heavy metals to provide an additional safety verification.
We test appearance (color, texture), taste and odor, solubility in water, flowability of powder, and moisture content.
Lymph Go must maintain quality throughout its shelf life. We conduct ongoing stability studies to ensure this:
Real-Time Stability: Batches are stored under normal conditions and tested at regular intervals (typically 3, 6, 12, 18, and 24 months) to confirm they maintain potency and quality.
Accelerated Stability: Product is stored under elevated temperature and humidity conditions to predict how it will perform over time. This helps establish appropriate shelf life and storage recommendations.
Stress Testing: Product is exposed to extreme conditions (light, heat, humidity) to identify potential degradation pathways and ensure packaging provides adequate protection.
These studies confirm that Lymph Go maintains its potency and safety throughout its recommended shelf life when stored as directed.
While our internal quality control is rigorous, we believe in additional verification through independent third-party laboratories. These labs have no financial interest in test results—they simply report what they find.
Why Third-Party Testing Matters:
Third-party laboratories verify label claim accuracy (ingredients and amounts), screen for undisclosed fillers or adulterants, test for contaminants (heavy metals, microorganisms), confirm absence of prohibited substances, and validate our internal test results.
Beyond product testing, our manufacturing facilities maintain certifications from respected industry organizations:
NSF International: NSF certification for dietary supplements demonstrates compliance with stringent quality standards covering facility design, personnel training, quality systems, and product testing.
USP Verification (Where Applicable): The United States Pharmacopeia sets quality standards for dietary supplements. USP verification confirms products meet these pharmaceutical-grade standards.
Before Lymph Go was brought to market, each ingredient underwent comprehensive safety evaluation:
Historical Use Review: We examined centuries of traditional use for each botanical ingredient, looking for safety concerns or contraindications.
Published Safety Data: We reviewed peer-reviewed studies on ingredient safety, including clinical trials, toxicology studies, and case reports.
GRAS Status: Where applicable, we confirmed ingredients have Generally Recognized as Safe (GRAS) status from relevant authorities.
Interaction Potential: We assessed potential interactions with common medications, other supplements, and medical conditions.
Safety monitoring continues after products reach the market:
Adverse Event Reporting: We maintain systems for customers and healthcare providers to report any adverse events or unexpected effects. All reports are investigated promptly.
Trend Analysis: We analyze patterns in customer feedback to identify any potential safety signals early.
Literature Monitoring: Our team continuously reviews new research publications for emerging safety information about ingredients.
Regulatory Compliance: We fulfill all legal requirements for adverse event reporting to the FDA and other regulatory authorities.
Although we work diligently to prevent quality issues, we maintain comprehensive recall procedures should they become necessary:
Clear protocols exist for initiating recalls quickly if quality or safety issues are discovered. We maintain detailed distribution records allowing rapid identification of affected batches. Customers are notified through multiple channels if their product is affected. Full refunds are provided for recalled products.
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