White label
Our existing formulations with your branding. The fastest route to a shelf-ready product.
Explore white labelElectrolyte and hydration supplement manufacturing
GMP-certified, FDA-registered production in Canada and the United States. Formulation, compliance, packaging, and production run by one team.
Evo Hydration manufactures electrolyte and hydration powders for other brands. You bring the brand, the audience, and the market you want to win. We handle formulation, regulatory work, packaging, and production.
Most of the brands we work with are already selling something successfully and want hydration added to the line without building a plant, hiring a formulator, or learning supplement law. Production runs from 1,000 units for a first pouch order up to 100,000 and beyond once a product proves itself.
Production capability
- Production range
- 1,000 to 100,000+ units
- The same formula and packaging scale up on reorder without requalification.
- Minimum order
- 1,000 units
- Jars, tubs, and stand-up pouches. Stick packs and sachets start at 20,000.
- Formats
- Stick packs, sachets, stand-up pouches, jars, tubs, cartons
- Boxed stick packs in counts of 10, 15, or 30 for retail and subscription.
- First production run
- 6 to 10 weeks
- Lead time for a first white-label or private-label run once artwork is approved. Custom formulation adds its development time, typically 8 to 12 weeks in total.
- Reorders
- 4 to 6 weeks
- Once artwork and specifications are approved, repeat runs skip the setup stages.
- Sampling
- 2 to 3 rounds
- Allow 3 to 4 weeks for bench-top samples to reach you for approval before anything is scheduled.
- Typical project budget
- From $15,000 USD
- Covers formulation, packaging, compliance, and the first production run.
How the partner network works
We work as an extension of our partner manufacturers. Every facility in the network is GMP-certified and FDA-registered, and we place each project with the plant built for it.
That placement comes down to your product type, your volume, the certifications you need, and your timeline. A 1,000-unit pouch run for a DTC launch and a 100,000-unit stick pack order for retail distribution are different jobs that belong on different lines. Working across several facilities is what lets us match your category and budget instead of forcing every run onto one line.
What stays constant is who you deal with. We hold the manufacturer relationships and run production end to end: scheduling, quality checkpoints, certificates of analysis, and logistics. You get one point of contact, one quote, and one invoice.
What happens to your formula before it runs
Every formulation goes through third-party testing for purity, potency, and label accuracy before a production run is released. That covers heavy metals, microbial contamination, and whether the panel on the box matches what is in the powder.
Electrolyte powders fail in specific, predictable ways. They clump when moisture control slips. They separate when particle sizes are not matched. They lose potency when a mineral form was chosen for cost rather than stability. Our R&D team runs accelerated and real-time shelf-life testing so those problems surface on a bench, not in a customer's kitchen.
You see two to three rounds of bench-top samples, about three to four weeks in, before anything is scheduled for production. Taste, mixability, and appearance all get signed off by you first.
Regulatory work is part of the build
A compliant label is not a step you bolt on at the end. Ingredient choices, dosages, and claims all have regulatory consequences, and catching them after a formula is locked is expensive.
The FDA caps supplemental potassium at 99 mg per serving. Health Canada requires an NPN for Natural Health Products and has its own view of permitted claims. A product built for both markets can share one bilingual label and one SKU, but only if it was designed that way from the start.
Our regulatory team builds the supplement facts panel from your finished formula, reviews every claim for substantiation, and prepares the documentation your buyers and importers ask for.
Quality and certification
- GMP certified
- Every partner facility
- Current Good Manufacturing Practice, audited by a third party on a recurring schedule.
- FDA registered
- Every partner facility
- Registered as a dietary supplement manufacturing establishment.
- Third-party testing
- Purity, potency, label accuracy
- Run on every formulation before a production run is released.
- Optional certifications
- Kosher, Halal, NSF, organic
- Available depending on the formula and the facility your project is placed with.
Where your product is made
- Canada
- British Columbia, Ontario
- United States
- California, Utah, Texas, Georgia
- China
- Export and cross-border e-commerce volumes
Regulatory coverage
- United States
- FDA, DSHEA
- Supplement facts panels, ingredient and allergen declarations, claims review.
- Canada
- Health Canada, NHP and NPN
- Natural Health Product submissions and bilingual labelling for a single cross-border SKU.
- European Union
- Supported
- Compliance support for brands selling into multiple regions at once.
- Export markets
- Documentation only
- Registration in your destination market stays with you or your importer of record.
Documentation you receive
Retail buyers, distributors and importers each ask for a different subset of these. We prepare the full set so you are not chasing paperwork mid-negotiation.
- Certificate of free sale
- Certificate of origin
- Certificates of analysis
- Ingredient and allergen declarations
- Product specification sheets
Pick the service that fits
Private label
Adjust ingredients, dosages and flavours on one of our base formulas so the product is yours.
Explore private labelCustom formulation
Built from scratch by our R&D team. You hold the intellectual property on the finished formula.
Explore custom formulation
Frequently asked questions
All questionsWe work as an extension of our partner manufacturers. We hold the relationships, place your product with the facility built for it, and run the production end to end: scheduling, quality checkpoints, certificates of analysis, and logistics. Working across several facilities is what lets us match your category, certifications, and budget rather than forcing every run onto one line. You deal with one team throughout.
Every partner facility is GMP-certified and FDA-registered, and all of them undergo regular third-party audits. Kosher, Halal, NSF, and organic certifications are available depending on your product requirements and which facility your project is placed with. We confirm the certifying body before production starts.
1,000 units for jars, tubs, and stand-up pouches. Stick packs and sachets start at 20,000 because of how the filling equipment is set up. Most first-time brands start with pouches to keep the initial commitment low, then move to stick packs once demand is proven.
Six to ten weeks from approved artwork to delivered product for white-label and private-label runs, with sampling taking three to four weeks before that. Custom formulation takes eight to twelve weeks in total because the formula is developed first. Reorders on approved artwork ship in four to six weeks.
Yes. We arrange facility tours for prospective and existing clients. Tell us where you are and what you want to see, and we will set it up with the relevant partner.
With custom formulation, yes. The formula is yours and you hold the intellectual property. We manufacture it for you. With white-label you are using a formulation from our existing library, and with private-label you are modifying one, so those stay ours while your branding, artwork, and flavour direction remain yours.
Yes, and it is worth planning for at the formulation stage. Our team works across both countries with direct manufacturer, ingredient supplier, and regulatory relationships in each. A product designed for both markets can run as one bilingual SKU rather than two separate production runs.
Certificates of analysis for the finished product covering purity, potency, and label accuracy. For export we also prepare a certificate of free sale, certificate of origin, ingredient and allergen declarations, and product specification sheets. Retail buyers and importers generally ask for some combination of these.
Talk to us about your product
Tell us your format, target market, and volume. We will come back with a production assessment and a quote.