Powder Manufacturing
POWDER MANUFACTURING
The Benefits of Powders

Easy
Consumption
Powdered formats eliminate swallowing difficulties, making them accessible to a wide audience across all age groups. When mixed with liquids or food, they offer flavor flexibility and easy ingestion, particularly valuable for individuals with dysphagia or other medication compliance challenges.
Maximum
Flexibility
Powder formulations offer exceptional dosing flexibility, allowing consumers to adjust serving sizes to meet individual needs. This adaptability makes powders well-suited for pediatric, geriatric, and clinically supported applications requiring specific dosage requirements.
Superior
Bioavailability
Pre-dissolved powders ensure efficient absorption. Clinical studies demonstrate excellent bioavailability profiles, particularly beneficial for compounds requiring rapid systemic availability.
Large
Dosages
Powder formulations accommodate significantly higher dosage levels per serving, making them ideal for clinically studied compounds that require substantial daily intake. This format efficiently delivers larger quantities of active ingredients without the bulk constraints of other delivery methods.

Easy Consumption
Powdered formats eliminate swallowing difficulties, making them accessible to a wide audience across all age groups. When mixed with liquids or food, they offer flavor flexibility and easy ingestion, particularly valuable for individuals with dysphagia or other medication compliance challenges.
Maximum Flexibility
Powder formulations offer exceptional dosing flexibility, allowing consumers to adjust serving sizes to meet individual needs. This adaptability makes powders well-suited for pediatric, geriatric, and clinically supported applications requiring specific dosage requirements.
Superior Bioavailability
Pre-dissolved powders ensure efficient absorption. Clinical studies demonstrate excellent bioavailability profiles, particularly beneficial for compounds requiring rapid systemic availability.
Larger Dosages
Powder formulations accommodate significantly higher dosage levels per serving, making them ideal for clinically studied compounds that require substantial daily intake. This format efficiently delivers larger quantities of active ingredients without the bulk constraints of other delivery methods.
The Benefits of Powders

Easy Consumption
Powdered formats eliminate swallowing difficulties, making them accessible to a wide audience across all age groups. When mixed with liquids or food, they offer flavor flexibility and easy ingestion, particularly valuable for individuals with dysphagia or other medication compliance challenges.
Maximum Flexibility
Powder formulations offer exceptional dosing flexibility, allowing consumers to adjust serving sizes to meet individual needs. This adaptability makes powders well-suited for pediatric, geriatric, and clinically supported applications requiring specific dosage requirements.
Superior Bioavailability
Pre-dissolved powders ensure efficient absorption. Clinical studies demonstrate excellent bioavailability profiles, particularly beneficial for compounds requiring rapid systemic availability.
Larger Dosages
Powder formulations accommodate significantly higher dosage levels per serving, making them ideal for clinically studied compounds that require substantial daily intake. This format efficiently delivers larger quantities of active ingredients without the bulk constraints of other delivery methods.
What Sets Eva Nutra Apart From the Rest?
Blending
Quality Testing
Packaging
Blending
Quality Testing
Packaging

Our Bohle blending technologies use enhanced processes to provide a uniform mixture of dry powder batches. The blending process can be scaled for quantities ranging from four to 12,000 liters to deliver optimal production results.

Our relentless quality check begins the moment ingredients are received at Eva Nutra. After verification, raw materials undergo screening for odors, heavy metals, bacterial presence, and identified contaminants. These rigorous tests ensure that the final products consist solely of what is stated on the label.

Eva Nutra operates high-speed packaging lines offering bulk containers and custom retail options. Our flexible packaging systems accommodate weights ranging from 1g to 1000g, operating at speeds of 40+ units per minute.

Our Bohle blending technologies use enhanced processes to provide a uniform mixture of dry powder batches. The blending process can be scaled for quantities ranging from four to 12,000 liters to deliver optimal production results.

Our relentless quality check begins the moment ingredients are received at Eva Nutra. After verification, raw materials undergo screening for odors, heavy metals, bacterial presence, and identified contaminants. These rigorous tests ensure that the final products consist solely of what is stated on the label.

Eva Nutra operates high-speed packaging lines offering bulk containers and custom retail options. Our flexible packaging systems accommodate weights ranging from 1g to 1000g, operating at speeds of 40+ units per minute.
This chart represents our most popular powder manufacturing options.
Please call 1-888-828-7732 to explore additional options.
3rd Party Certified
Dedicated to going above industry standards
We are GMP Audited/Certified by USP and NSF to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP audited lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.
Learn More
United States Pharmacopeia (USP)
- Founded in 1820 to protect patients from poor-quality medicine.
- USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
- Re-test/Spot Checks are conducted 1-6 times per year using samples purchased in stores.
- USP may perform testing beyond specified tests.
- Tests for dissolution and disintegration.
- USP can conduct unannounced audits to check for compliance.
NSF International
- NSF provides GMP registration and NSF/ANSI 455 certification for dietary supplements, cosmetics, personal care products and OTC drugs.
- GMP certification and registration provides consumers and retailers with assurance that your product is manufactured utilizing industry best practices.
- These standards encompass regulatory requirements, retailer quality requirements and industry best practices and are designed to strengthen safety, quality and trust throughout the supply chain.
- NSF can also Certify individual products. NSF certifies products against NSF/ANSI 173, the only American National Standard that establishes requirements for the ingredients in dietary and nutritional supplements.
Dedicated to going above industry standards
We are GMP Audited/Certified by USP and NSF to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP audited lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.
Learn More
United States Pharmacopeia (USP)
- Founded in 1820 to protect patients from poor-quality medicine.
- USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
- Re-test/Spot Checks are conducted 1-6 times per year using samples purchased in stores.
- USP may perform testing beyond specified tests.
- Tests for dissolution and disintegration.
- USP can conduct unannounced audits to check for compliance.
NSF International
- NSF provides GMP registration and NSF/ANSI 455 certification for dietary supplements, cosmetics, personal care products and OTC drugs.
- GMP certification and registration provides consumers and retailers with assurance that your product is manufactured utilizing industry best practices.
- These standards encompass regulatory requirements, retailer quality requirements and industry best practices and are designed to strengthen safety, quality and trust throughout the supply chain.
- NSF can also Certify individual products. NSF certifies products against NSF/ANSI 173, the only American National Standard that establishes requirements for the ingredients in dietary and nutritional supplements.
View Our 3D Lab Tour!
View Our 3D Lab Tour!
Powder Specifications
Flavoring |
---|
Unflavored, Berry Flavors, Citrus Flavors, Tropical Flavors, Custom Flavors |
Powder Appearance |
White/Off-White, Green (Matcha/Spirulina), Pink/Red (Beet Root Powder), Orange (Turmeric Base), Tan/Beige (Protein/Fiber) |
Packaging |
Small Containers (50g-100g), Medium Containers (100g-300g), Large Jars/Tubs (1-5lbs) |
This chart represents our most popular powder manufacturing options. Please call 1-888-828-7732 to explore additional options.
3rd Party Certified
Dedicated to Going Above Industry Standards

We are GMP Audited/Certified by USP and NSF to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP audited lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.
- Founded in 1820 to protect patients from poor-quality medicine.
- Before DSHEA, USP set the standards for acceptable “Nutritional supplements”
- Launched Dietary Supplement Verification Program in 2001 to combat quality inconsistencies in the market.
- USP focuses on Health Products (Pharmaceutical & Dietary Supplements)Formation of DSHEA recognized USP-NF standard as official but voluntary.
- USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
- Retest/Spot Check conducted 1-6 times per year using samples purchased in stores.
- USP may preform testing beyond specified test on if there is probability that the product contains known contaminants.
- Tests for dissolution and disintegration.
- USP can conduct unannounced audits to check for compliance.
View Our 3D Lab Tour!
Why Choose Eva Nutra as Your Private Label Contract Manufacturer?
Why Choose Eva Nutra as Your Private Label Contract Manufacturer?
Frequently Asked Questions
Frequently Asked Questions
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