Product Management Group
FDA-registered R&D laboratory for supplement and beauty product formulation
From ideation to your first sale

Private Label Manufacturing for beauty, supplements & wellness brands.

PMG takes health, wellness, beauty and nutraceutical brands from concept to shelf — R&D, manufacturing, certifications, packaging, distribution, fulfillment and channel development under one roof.

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010203040506R&DManufacturingCertificationsPackagingDistributionSales Channels
01R&D
Formulation chemistry, prototyping & ingredient sourcing

Our clients' products sit on shelves at major big-box retailers and ship daily through the largest online marketplaces in North America.

What we specialize in

We specialize in turnkey contract manufacturing for beauty, wellness, personal care and nutraceutical brands — from research and development through first sale, with partner facilities in five US states and a Miami gateway into Latin America.

Private label starts at 1,000 units and custom formulation at 5,000 units per SKU. Production runs in FDA (Food and Drug Administration)-registered, GMP (Good Manufacturing Practice)-compliant facilities, with MoCRA (Modernization of Cosmetics Regulation Act)-compliant operations for cosmetics. See the full FAQ.

The full-stack difference

Where most manufacturers hand you a pallet and wish you luck, we keep going.

Most contract manufacturers will formulate a great product and ship you a pallet. Then it's your problem. Find a 3PL. Negotiate Amazon FBA. Land a retail meeting. Eat the cost of dead inventory. PMG is built differently. We don't stop at the warehouse door — we stay with you until your product is in a customer's hands.

Where competitors stop — where PMG begins
Where most contract manufacturers end
Formulation, manufacturing, a pallet at the dock.
Where PMG keeps going
Distribution, fulfillment, and channel sales through to first customer.

One partner. One point of accountability. From the first sketch on a napkin to the first unit that reaches a paying customer.

GMP-compliant contract manufacturing facility line for private label supplement and skincare production
Why brands choose PMG

Three reasons brands trust us with the whole journey.

Full value chain

Full-stack — not just manufacturing

Other contract manufacturers stop at the warehouse door. We carry your product through distribution, fulfillment, and into the sales channels where it actually sells. You get one accountable partner instead of five vendors pointing fingers at each other.

1,000 unit minimum

Built for startups, scaled for retail

Our MOQ starts at 1,000 units on private label stock formulas and 5,000 units for custom formulations — low enough for first-time inventors to launch without taking on warehouse-sized risk. The same infrastructure scales seamlessly when your product hits big-box retail.

USA → LATAM

USA-wide, with Miami as your LATAM gateway

Headquartered in Florida with partner facilities in FL, NC, TX, MN, and AZ, we service the entire United States. Because we're built around Miami — the natural commercial gateway to Latin America — we can take your product across the LATAM border in ways most domestic manufacturers cannot.

Our wedge — and our wheelhouse

Specialists in health, wellness, personal care, beauty, and nutraceuticals.

These are the categories we know cold. Decades of combined formulation experience across our team, FDA (Food and Drug Administration)-registered partner facilities, GMP compliance, and a deep network of chemists, regulatory specialists, and packaging partners. Whether you're launching a clean skincare line, a probiotic supplement, a body care brand, or a wellness category innovator, we've built products like yours before — and we know what it takes to get them on a shelf and into a customer's cart.

Finished product samples from nutraceutical, skincare, and personal care contract manufacturing

Skincare & Beauty

Serums, moisturizers, cleansers, treatments

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Sun Care & SPF

Mineral and chemical formulations, OTC-compliant

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Nutraceuticals & Supplements

Capsules, tablets, gummies, powders, liquids

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Personal Care

Body care, hair care, oral care

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Wellness & Aromatherapy

Essential oils, blends, functional formulas

Explore

OTC & Specialty

Topical pain relief, first aid, sanitization

Explore

Don't see your category? We've also produced in Apparel, Soft goods, Specialty & Customized Branded Accessories. Let's talk about your project.

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The Miami advantage

Your gateway to 650 million consumers across Latin America.

Most US contract manufacturers ship within the lower 48 and stop there. PMG was built differently. Miami sits at the natural commercial crossroads between North America and Latin America — and our team has spent decades building the regulatory, logistics, and distribution network to move product across that border efficiently and compliantly.

If your growth roadmap includes Mexico, Central America, the Caribbean, or South America, you don't need a separate partner for each region. You need a manufacturer who already speaks the language — literally and operationally — and who can build LATAM channel readiness into your product from day one.

  • Customs, labeling, and regulatory documentation built into your product spec from day one
  • Established 3PL and distribution relationships in key LATAM markets
  • Bilingual project management across every stage of your engagement
Learn about our LATAM capabilities →
Our engagement process

A clear path from your first call to your first sale.

Request a Consultation →
Where our clients' products live

On the shelves you're trying to reach.

Our clients' products are sold by major big-box retailers and ship daily through the largest online marketplaces in North America. Our team has spent decades earning the trust of buyers, regulators, and consumers across the Americas. We don't publicly name the brands or retailers we serve — confidentiality is part of what our clients buy from us.

Finished private label beauty and personal care products on retail shelves at major retailers
Channels we ship into
WalmartTargetCostcoAmazonSpecialty RetailDTC FulfillmentLATAM Distribution
Operational — every product, every run
FDA-registered facilitiesGMP-compliant productionMoCRA-compliant operations
Available across our facility network on request
USDA OrganicKosherHalalVegan formulationsCruelty-FreeGluten-FreeAllergen-conscious manufacturing
What these regulatory terms mean
FDA
Food and Drug Administration — US federal regulator for food, supplements, cosmetics and drugs
cGMP
Current Good Manufacturing Practice — the FDA's manufacturing quality regulations (21 CFR)
MoCRA
Modernization of Cosmetics Regulation Act — US cosmetics registration and safety law
COFEPRIS
Federal Commission for the Protection against Sanitary Risk — Mexico
ANVISA
National Health Surveillance Agency — Brazil
INVIMA
National Institute of Food and Drug Surveillance — Colombia

Certifications vary by product category and manufacturing facility.

Where we manufacture

Contract manufacturing from Florida, across five states.

PMG is headquartered in Boca Raton, Florida, with Miami serving as our gateway to Latin America. Production, packaging, and fulfillment run through partner facilities in Florida, North Carolina, Texas, Minnesota, and Arizona — one team and one point of accountability behind all of them.

Florida
Headquarters in Boca Raton and the Miami gateway to Latin America
North Carolina
Mid-Atlantic and Southeast logistics
Texas
Southwest fulfillment and LATAM-adjacent operations
Minnesota
Midwest logistics and specialty manufacturing
Arizona
Western US fulfillment and West Coast distribution
Locations

Contract manufacturing in Miami and Boca Raton

Our Florida headquarters, the facility network, and why South Florida is the LATAM gateway.

Startup resources

Low MOQ supplement manufacturing from 1,000 units

What the lowest minimums actually mean, and which formats support them.

Markets

USA to LATAM expansion

Manufacture in the USA, register and distribute across Mexico, Brazil, Colombia, and Chile.

Small batch beauty manufacturing →Texas contract manufacturing →Beauty product manufacturing in Florida →
The PMG Journal

Guides for brands planning their first run.

Partner selection

How to Choose a Private Label Manufacturing Partner

10 questions to ask before you sign, plus a free evaluation checklist.

Read the article →
Volume planning

MOQ and Manufacturing Volume: What Actually Matters

Why minimums exist, what they cost below volume, and how to plan a first run you can sell through.

Read the article →
Cost planning

How Much Does It Cost to Manufacture Supplements?

A phase-by-phase breakdown of R&D, ingredients, production, packaging, and compliance costs.

Read the article →
View all articles →
Frequently asked questions

The questions inventors and brand founders ask us first.

Contract manufacturing is when a brand hires an outside partner to produce its product instead of building and running its own facility. The brand owns the product, the formula, and the label; the manufacturer handles sourcing, production, quality control, and packaging. For beauty and wellness brands it means launching a compliant, retail-ready product without the capital cost of a factory.

Private label products built on our existing stock formulations can run as low as 1,000 units. Fully custom formulations typically start at 5,000 units, because custom work carries formulation, testing, and raw material commitments that stock products do not. As your brand scales, we scale with you — there is no upper limit on what we can produce.

A private label launch using one of our existing FDA (Food and Drug Administration)-compliant formulas can move from contract to first production run in approximately 60 to 90 days. Custom formulations typically run 4 to 6 months depending on testing, certification, and regulatory requirements. Because we also handle packaging, distribution, and fulfillment, your first sale follows production rather than waiting on a second round of vendor sourcing.

Private label puts your brand on an existing, proven stock formula — fastest path, lowest minimum, least formulation risk. Modified stock starts from that same base and adjusts actives, sensory profile, or claims, which keeps most of the speed while giving you differentiation. Custom formulation develops a product from a target profile, which takes the longest and costs the most up front but produces something no competitor can order off a shelf.

The main drivers are formulation work, raw material and active ingredient selection, batch size, packaging components, and the testing and certification your category and markets require. Private label avoids most development cost because the formula and stability data already exist. Custom adds R&D, benchmark iterations, and stability testing before you ever run production — which is why volume has such a large effect on your per-unit cost.

Yes. We handle the customs documentation, labeling requirements, regulatory compliance, and distribution partnerships needed to move product into Mexico, Central America, the Caribbean, and South America, including COFEPRIS (Federal Commission for the Protection against Sanitary Risk – Mexico), ANVISA (National Health Surveillance Agency – Brazil), and INVIMA (National Institute of Food and Drug Surveillance – Colombia) registration pathways. Miami serves as our gateway to the region, and LATAM requirements are far cheaper to design in at formulation than to retrofit later.

Our partner facilities are FDA-registered and GMP (Good Manufacturing Practice)-compliant, with MoCRA (Modernization of Cosmetics Regulation Act)-compliant operations for cosmetics. Specific certifications are confirmed per product and per manufacturing facility before a project is placed.

Both. A meaningful portion of our work is with first-time inventors and startup brands launching their first product — our low private label minimums and full-service model exist precisely to make that path accessible. We also work with established brands launching line extensions or expanding into new geographies.

PMG covers the full value chain: research and development, manufacturing, packaging and component sourcing, product testing, certifications and compliance, distribution, 3PL fulfillment, Amazon FBA prep, and channel sales development. Most contract manufacturers stop at the warehouse door — you work with one partner from concept to your customer's hands.

The best fits are health, wellness, personal care, beauty, nutraceutical, and OTC products where the founder wants one partner across formulation, production, and getting to market. Tell us your category, your target volume, and your timeline through our project form, and we will give you an honest read on fit — including telling you when we are not the right partner.

Confirm the facility is FDA-registered and GMP (Good Manufacturing Practice)-compliant for dietary supplements, and ask which certifications apply to your specific format — capsules, tablets, gummies, powders, and liquids are not interchangeable capabilities. Check that the minimum order quantity matches your launch budget, and confirm you own the formula and the testing data. Finally, ask what happens after production, because packaging, distribution, and fulfillment are often left for the brand to solve alone.

Yes. We manufacture OTC formulations, including sun care and other monograph categories, through FDA-registered, GMP-compliant partner facilities. OTC work carries additional requirements — Drug Facts labeling, monograph alignment, and stability and testing obligations — so we scope those up front rather than discovering them mid-project.

Skincare, sun care, body care, and hair care are core categories for us, covered from R&D through packaging, testing, and retail-ready fulfillment. Our team includes formulation chemists and regulatory specialists with decades of individual experience in these categories, and our operations are MoCRA (Modernization of Cosmetics Regulation Act)-compliant.

Yes — bilingual project management is a baseline, not a premium. Our team operates in English and Spanish with working Portuguese capability for Brazilian market engagements, which matters because regulatory submissions in Mexico and Brazil are done in the local language.

Available capabilities across our partner facility network include USDA Organic, Kosher, Halal, vegan formulations, Cruelty-Free, Gluten-Free, and allergen-conscious manufacturing, on top of FDA-registered and GMP-compliant production. Certifications vary by product and by facility, so we confirm which ones apply to your specific formula before production.

Our headquarters is in Boca Raton, Florida, and we operate through a network of partner manufacturing and distribution facilities in Florida, North Carolina, Texas, Minnesota, and Arizona. That footprint gives us efficient logistics coverage across the entire United States, with Miami serving as the gateway to Central and South America.

We don't publish standard pricing, because a quote depends on format, formula, batch size, packaging components, and the testing and certifications your category and markets require. What we do is quote the whole path — formulation, production, packaging, testing, and fulfillment — so you are not surprised by a second and third vendor invoice later. Share your product, volume, and timeline and we'll come back with a scoped quote.

Payment terms are set per project in your quote and agreement, and they generally follow project milestones — development and testing, raw material and component purchasing, and production. Terms depend on batch size, component lead times, and whether the work is private label or custom, so we confirm them in writing before anything is ordered.

As a planning guide: discovery and scoping usually run a couple of weeks, formulation is fast for private label and the longest stage for custom work, testing and certification depend on your category, and production and packaging follow component lead times. Overall, a private label launch typically runs about 60 to 90 days from contract to first production run, and a custom formulation typically runs 4 to 6 months. We give you a dated schedule for your specific product at kickoff.

Production runs in FDA (Food and Drug Administration)-registered, GMP (Good Manufacturing Practice)-compliant facilities with batch records, identity testing, and quality control on every run, and you receive COA documentation for your batch. Product is manufactured to the specification you approve, and if a batch does not meet that approved specification we work the issue with you rather than handing you a testing report and a phone number.

Manufacturing is the middle of our scope, not the end. After production we handle packaging, distribution, 3PL fulfillment, Amazon FBA prep, and channel sales development, and your project lead stays with you through first sale. Reorders, documentation requests, and regulatory paperwork go through that same person.

Your formula, specification, and testing data are already documented after the first run, so repeat batches skip development and move straight to scheduling and component lead times. Scaling up usually improves your per-unit cost, and larger volumes can open formats or facilities that weren't practical at launch quantities. There is no upper limit on what the network can produce.

Most contract manufacturers stop at the warehouse door — they make the product and leave distribution, fulfillment, and channel work for you to source separately. PMG covers the whole value chain under one accountable team, starts at 1,000 units on private label stock formulas so first-time inventors can actually begin, and builds Latin American compliance in from formulation rather than retrofitting it after a US launch.

It depends on the category. Dietary supplements and cosmetics are not pre-approved by the FDA, but they must be manufactured, labeled, and substantiated to FDA requirements, with MoCRA (Modernization of Cosmetics Regulation Act) obligations applying to cosmetics. OTC drugs must align with an applicable monograph or a separate approval pathway, and Latin American markets require registration with COFEPRIS, ANVISA, or INVIMA before sale. We scope which of these apply to your product before production, not after.

Yes, and they vary by market and category. Labeling language, ingredient restrictions, permitted claims, product registration, and import documentation all differ country to country, and an ingredient that is routine in the US can be restricted elsewhere. That is why we design for your target markets at formulation and handle customs documentation and registration pathways through our Miami gateway.

Custom formulations typically start at 5,000 units per SKU, because custom work carries formulation, testing, and raw material commitments that stock products do not. If that is above your launch budget, private label on a stock formula starts at 1,000 units, and a modified stock formula is often the middle path — real differentiation without a full custom minimum.
Ready to start?

Tell us about your product. We'll tell you what's possible.

Every great brand starts with a single conversation. Share a little about your idea, your target market, and your timeline, and one of our project consultants will reach out within one business day with a clear next step.

Step 1 of 2Project basics

This decides which questions we ask in step 2.

Production budget.

What's the product? Who's it for? What problem does it solve?

Contact information

If your brand doesn't have a name yet, 'TBD' is fine.

Your answers save as you go, so you can finish later if you need to.