Private Label Supplements · Hauppauge, New York
Private Label Supplements from a Catalog of 300+ Ready Formulas
Put your brand on a supplement or personal care product that is already developed, already in the market through other brands, and already made in our own FDA-registered New York facility on botanical extracts we produce ourselves. Published minimum order quantities. No offshore supply chain in between.
- Published minimum order quantities. 5,000 units for liquids and personal care, 2,500 for liquids 8 oz and larger. Every number on this page is printed, not “available on request”.
- We make the botanical extracts. Sourced globally and made in New York since 1972, so the ingredient supply behind your formula is ours, not a broker’s.
- One US site, supplements and personal care. NSF GMP, FSSC 22000, FDA-registered, USDA Organic, Kosher and Halal, all under one roof in New York.
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NSF GMP
FSSC 22000
FDA-registered facility
USDA Organic
Kosher
Halal
Botanicals sourced globally
Extracts made in New York since 1972
1972
Extracting botanicals since
160,000
Sq ft FDA-registered NY facility
5,000
Unit minimum order quantity, liquids and personal care
300+
Ready private label formulations
What are private label supplements?
Private label supplements are finished products a manufacturer has already developed, which a brand buys and sells under its own name. The formula, the process and the specification belong to the manufacturer. You choose the product, the label and the pack, and you own the customer.
That is the whole appeal: the hard part — formulation, stability, sourcing, a validated process — is already finished. What you are buying is speed to market and a shorter list of things that can go wrong on your first run.
Private label vs contract manufacturing
The two terms get used loosely by vendors, which is why buyers arrive confused. The only question that actually matters is how much of the formula you control.
| Route | Who owns the formula | What you decide | Who it suits |
|---|---|---|---|
| Private label | The manufacturer, from an existing catalog | Which product, the label, the packaging, and often the pack size or flavor | A brand launching quickly on a proven base |
| Contract manufacturing | You, or you and the manufacturer jointly | Ingredients, dosage, format, specification, testing plan | A brand with its own formula or a differentiated product |
If the product you want already exists in a catalog, private label is the right route and this is the right page. If it does not exist yet, you want contract manufacturing for supplements instead — the same facility, the same quality system, a different starting point.
Grand View Research values the US dietary supplement contract manufacturing market at USD 6.65 billion in 2025, reaching USD 16.6 billion by 2033 at a 12.2% CAGR (Grand View Research). Most of that is brands who would rather own the brand than the plant.
What is in the BioB private label supplement catalog?
More than 300 existing private label formulations across liquid supplements, capsules, tablets, powders, oral care, pet wellness and personal care. Liquids are the deepest part of the catalog, including alcohol-free formats. You can browse the whole range before you ever speak to us.
Liquid supplements
Our specialty since 1972. Extracts, tinctures, syrups and liquid shots, in dropper, spray and standard closures. This is the format we control end to end, because we make the extract as well as the finished bottle.
Browse liquid supplements →Alcohol-free liquids
Alcohol-free extract formats for ingestible products, for brands whose category, retailer or customer will not accept an ethanol-carried tincture. Few private label suppliers offer this as a stock option.
Browse alcohol-free liquids →Capsules
Two-piece capsules filled from existing catalog formulations. A high-volume format for us. See the minimum order quantities below before you plan around it.
Browse capsule products →Tablets
Compressed tablets from the catalog, including coated presentations. Also a high-volume format, with the same minimum order quantity as capsules.
Powders
Powder blends for canister or stick-pack presentation, drawn from existing formulations. Minimum order quantities are confirmed at quote because they move with the pack.
Oral care
Oral care products made under the same quality system as the supplement lines, for brands extending beyond the capsule aisle.
Browse oral care products →Pet wellness
Pet wellness formulations, most naturally in liquid form, for brands adding a companion-animal line to an existing human range.
Browse pet wellness products →Personal care
Serums, lotions, creams, sprays and oils from the same site, so a supplement brand can add a companion topical without adding a second vendor. See private label skin care manufacturing and serum manufacturing.
Browse personal care →Browse the catalog before you call
Most private label suppliers answer “what do you have?” with a contact form. We answer it with a list. The full range is published on the site, so you can shortlist products, then send us the ones you want formulation sheets and pricing for.
What are the minimum order quantities for private label supplements?
Liquids and personal care under 8 oz start at 5,000 units. Liquids 8 oz and larger start at 2,500 units. Capsules and tablets require 300,000 units total. Other formats are confirmed at quote. These are printed so you can qualify us in a minute.
| Format | Minimum order quantity | Notes |
|---|---|---|
| Liquids and personal care, under 8 oz | 5,000 units | Liquid extracts, alcohol-free formats, serums, lotions, creams and sprays |
| Liquids and personal care, 8 oz and larger | 2,500 units | Applies to 8 oz and 16 oz fills |
| Capsules | 300,000 units total | Counted across the production run rather than per bottle count |
| Tablets | 300,000 units total | Counted across the production run rather than per bottle count |
| Powders, oral care, pet wellness and other formats | Confirmed at quote | Driven by fill size, packaging format and blend complexity |
| Lead time | About 12 weeks | From approved formula and packaging to finished goods; packaging component availability is the usual reason a project runs long |
Three ways to launch a private label supplement
Take a catalog formulation exactly as it is, take a catalog formulation and change one thing about it, or have a product developed from scratch. The three routes differ in how long they take and how much of the formula ends up being yours.
1. Catalog, as it is
Choose a formulation from the 300+ already in production, approve the specification, and put your label on it. Nothing about the formula changes, so there is no development work and no formulation risk. This is the fastest route to a first pallet.
Best for: a first product, a line extension, or a brand testing a category before committing.
2. Catalog, with a modification
Start from a catalog base and change the flavor, the strength, the pack size, or an ingredient. The base is already qualified, so the work is a modification rather than a formulation program, and the documentation trail is shorter.
Best for: a brand that needs a point of difference but not a new formula. We will tell you at enquiry which side of the private-label line your change falls on.
3. Full custom
A product developed to your specification from the ground up, whether you bring the specification or we develop it with you from a benchmark. Longer, more involved, and the result is genuinely yours.
Best for: a differentiated product that does not exist in anyone’s catalog. Read contract manufacturing for supplements for how that route works.
How do I choose a private label supplement manufacturer?
Run the same ten questions past every vendor on your shortlist: published minimum order quantities, who owns the formula, where the botanical ingredients come from, which certifications are audited, what documents arrive with each lot, and who carries which regulatory duty. A vendor who will not answer these in writing before a quote will not answer them after one.
This is a checklist, not a ranking. Score each vendor yourself — including us.
- 1. Are the minimum order quantities published, or hidden behind a form? A supplier who will not print a minimum order quantity is either quoting each buyer differently or does not want you to know the number until you are invested. Ours are in the table above.
- 2. Who owns the formula, and what happens if you leave? In private label the manufacturer owns it — that is the trade you are making for speed. Make sure it is stated, not assumed, so a future move does not come as a surprise.
- 3. Where do the botanical ingredients come from? Ask whether the supplier makes them, buys them domestically, or imports them. That answer determines your exposure to tariffs, shortages and quality drift on the ingredients that matter most.
- 4. Is the facility FDA-registered, and is the GMP certification third-party audited? “GMP compliant” is a self-description. A named certifier is a verifiable fact. Ask which body issued it and ask to see the certificate.
- 5. What is tested on every lot, and do you receive the results? The right answer is a specification agreed before production and a Certificate of Analysis against it for each lot — not testing decided after the fact.
- 6. Can a catalog formula be modified, and when does that become custom? A supplier who says “anything is possible” is deferring the bad news. You want the boundary drawn at enquiry, before you build a launch plan on it.
- 7. Who does the label, and who is liable if it is wrong? Get the split in writing: who supplies the ingredient and specification data, who designs, who signs off, and who is answerable to FDA for what is printed.
- 8. What happens to the schedule when packaging slips? On a private label project the formula is not the bottleneck — bottles, closures and cartons are. Ask how a component delay is handled, because it will happen.
- 9. Can the same vendor make your companion products? If a topical, an oral care product or a pet line is anywhere in your two-year plan, one vendor across all of it means one quality system and one documentation package.
- 10. Will they tell you what you are responsible for? A supplier who leaves you believing they carry all of the regulatory duty is setting you up. The honest ones explain the split under 21 CFR Part 111 before you sign — see the section below.
We make the botanical extracts inside the formula
BioB Manufacturing is the finished-goods arm of Bio-Botanica, which has sourced botanicals globally and made extracts in New York since 1972. When you private label a botanical formulation from our catalog, the botanical extract was produced in the same New York facility that fills your bottle. It was not bought from a broker.
That is unusual. Most private label supplement suppliers are fillers: they buy extracts on the open market, blend, fill and label. It works until the market moves. Then the ingredient is short, the price jumps, the specification quietly changes, and the brand whose name is on the label finds out last.
Controlling the extract changes three practical things for a private label buyer. Supply continuity is ours to manage rather than a supplier’s to explain. The identity and specification of the extract are documented from raw botanical through to finished bottle, in one quality system. And when you want to modify a catalog formula, the people who make the extract are in the same building as the people who will reformulate it.
For ingredients we do not make ourselves — vitamins, minerals, amino acids and specialty botanicals — you buy through Bio-Botanica’s purchasing volume rather than your own. That means volume pricing on raw materials from the first run, qualified suppliers already on file, and one quality system covering both the extracts we make and the ingredients we source.
- One site. 160,000 sq ft in Hauppauge, New York. No import step in the middle of your supply chain, no tariff surprise in the landed cost.
- One quality system. NSF GMP certified, FSSC 22000 food safety certified, FDA-registered facility, USDA Organic, Kosher and Halal, all covering the same site.
- One vendor for supplements and personal care. A supplement and its companion cream come off the same site, with one COA package.
We do not white label. Every lot is made fresh to order.
White label means pre-made stock on a shelf waiting for a label. We do not keep one. Your product is manufactured when you order it, so it ships with its full shelf life, every repeat run is made to the same specification, and nothing you sell has been sitting in someone else’s warehouse. It is one of the reasons retailers and marketplaces accept our documentation without a second look.
What happens from first call to shipped lot
Six steps, about 12 weeks from approved formula and packaging to finished goods. The order never changes; what moves the date is how much of the specification already exists when you arrive and how quickly packaging components can be secured.
1
Scope call
Product, format, volume and timing. We tell you plainly whether our minimum order quantities fit your plan and whether private label or custom is the right route.
2
Formula
Choose a formulation from our proven private label catalog, or we review the specification you bring and develop one to your benchmark.
3
Preliminary quote
Pricing, minimum order quantities, components and lead time, so you know the numbers before anyone makes a sample.
4
Samples and specification sign-off
You assess samples until you approve. The finished-product specification and the test panel are fixed in writing here. Nothing scales until the sample is the product you want to sell.
5
Label and artwork review
You supply the artwork. We supply the ingredient and specification data it has to reflect, and check the printed panel against the actual product before the run.
6
Production, QC release and documentation
Manufacture under NSF GMP, release against the agreed specification, and ship from New York with the Certificate of Analysis and documentation package for the lot. Repeat runs start at step five unless the specification has changed.
Quality, testing and the documents you actually receive
Every lot ships against an agreed specification with a Certificate of Analysis for that lot. The test panel is fixed at sign-off, so you know before production what will be tested and what the release criteria are, rather than discovering it when the first pallet arrives.
This matters more in private label than buyers expect. You did not develop the formula, so the specification document is the only place the product is defined for you. It is what your own quality file is built on, what your retailer will ask to see, and what you will be measured against if anything is ever questioned.
What comes with the product
A finished-product specification for the item you selected. A Certificate of Analysis for each lot, against that specification. Ingredient and formulation data sufficient for your label panel. Batch records retained by us and available to support your file.
What backs it up
An NSF GMP certified, FSSC 22000 food safety certified, FDA-registered facility in New York, with USDA Organic, Kosher and Halal certifications on the same site. Details are published on our standards and certifications page rather than described only on request.
We do not publish a test panel here, because the right panel depends on the product. What we will do is agree it in writing before your run and report against it for every lot.
Who is responsible under 21 CFR Part 111?
Both of you. BioB manufactures under Part 111. But a brand owner whose name is on the label is itself a manufacturer under Part 111, and under §111.75 it must qualify its supplier rather than rely on a Certificate of Analysis alone — confirming that COA with its own testing, documenting the qualification, and reconfirming it periodically.
This is the single most common misunderstanding among private label buyers, and it is easy to see why. You did not develop the formula, you do not run the equipment, and the supplier holds the certifications. It feels like the manufacturer carries the regulatory weight. Legally, it does not work that way.
Part 111 attaches to whoever manufactures, packages, labels or holds a dietary supplement. Holding the label puts you inside that definition. The consequence spelled out at §111.75 is that you cannot simply accept a supplier’s Certificate of Analysis as proof: you have to qualify the supplier first, verify the COA with your own testing, keep the documentation of that qualification, and revisit it periodically. Read it directly at the eCFR, 21 CFR Part 111.
| Responsibility | BioB Manufacturing | You, the brand owner |
|---|---|---|
| Manufacturing under Part 111 | Operates the GMP quality system, batch records and production controls at our facility | Not required to operate a plant, but still a manufacturer under Part 111 by virtue of holding the label |
| Specification | Provides the finished-product specification and manufactures to it | Reviews and formally accepts the specification as the definition of your product |
| Certificate of Analysis | Issues a COA for every lot against the agreed specification | Under §111.75, must not rely on that COA alone — confirm it with your own testing and document why the supplier is qualified |
| Supplier qualification | Supplies the certification, facility and specification evidence you need to build the file | Performs and documents the qualification, and reconfirms it periodically |
| Label content and claims | Supplies the ingredient and specification data the panel must reflect; reviews artwork against the product | Owns the finished label, the claims made on it, and the substantiation behind them |
| Adverse event reporting | Supports investigation with batch and production records | Holds the reporting obligation as the firm whose name is on the label |
We cannot do your supplier qualification for you — the regulation deliberately puts it on you. What we can do is make it short: published certifications, a specification you receive before production rather than after, a COA on every lot, and a straight answer when your quality consultant emails with a question.
Why brands choose BioB for private label supplements
A catalog deep enough to launch from, minimum order quantities a small brand can meet, botanical extracts we make ourselves, and one US facility covering supplements and personal care. Plus a supplier who tells you where your own liability sits.
We make the botanical extracts
Botanical extraction in house since 1972, in the same building as the filling line. Sourced globally, made in New York, so traceability starts with us, not a broker.
Made fresh to order
No white label stock. Every lot is manufactured when you order it and ships with its full shelf life.
Minimum order quantities in print
5,000 units for liquids and personal care, 2,500 for liquids 8 oz and larger, 300,000 for capsules and tablets. Qualify us in a minute, not after three calls.
One US site
A single 160,000 sq ft FDA-registered facility in New York. No import step, no tariff variable, no offshore transit between you and a stockout.
Supplements and personal care together
Liquids, capsules, tablets, powders, oral care and pet wellness alongside serums, creams, lotions and sprays. One vendor, one quality system, one documentation package.
We tell you what you own
The 21 CFR Part 111 responsibility split is on this page, before the quote. You should know your obligations before you sign, not after.
Private label supplement FAQs
What are private label supplements?
Private label supplements are finished products a manufacturer has already developed and offers to brands to sell under their own name. The manufacturer owns the formula and the process; you choose the product, the label and the packaging. It is the fastest route to market because the formulation work is already done.
What is the difference between private label and contract manufacturing?
Private label means putting your brand on a formula the manufacturer already owns, chosen from a catalog and adjusted in label, packaging and often pack size. Contract manufacturing means the product is made to your specification, whether you bring the formula or develop it with us. The dividing line is how much of the formula you control.
What are your minimum order quantities?
Liquids and personal care under 8 oz start at 5,000 units. Liquids 8 oz and larger start at 2,500 units. Capsules and tablets require 300,000 units total. Powders, oral care, pet wellness and lozenges are confirmed at quote.
Can a smaller brand start with BioB?
Yes. 5,000 units of a liquid or personal care product is a launch quantity, not a factory quantity, and an 8 oz or 16 oz liquid can start at 2,500. Capsules and tablets are not a small first order at 300,000 units total, and we would rather tell you that before you spend time on a quote.
What is in your private label catalog?
More than 300 existing private label formulations, covering liquid supplements including alcohol-free formats, capsules, tablets, powders, oral care and pet wellness. You can browse them on our all products page and in the product directory before contacting us, then tell us which ones you want formulation sheets and pricing for.
Can I modify a stock formula?
Usually yes. Flavor, strength, pack size and some ingredient changes can be made to an existing base, which keeps the development work far shorter than a ground-up formulation. Larger changes move the project into contract manufacturing. We will tell you which side of that line your request falls on before quoting.
Do you help with label design and compliance?
We supply the ingredient and specification data your label has to reflect, and we review your artwork against the actual product before it is printed. Label design itself and the final compliance sign-off stay with you as the brand owner, because you are the party answerable for what is printed on the panel.
Do you provide a Certificate of Analysis for each lot?
Yes. Every lot ships with a Certificate of Analysis against the specification agreed for your product. The test panel is fixed in that specification, so you know at sign-off what will be tested and what the release criteria are, rather than finding out when the first pallet arrives.
Who is responsible under 21 CFR Part 111?
Both parties. BioB manufactures under Part 111. But a brand owner whose name is on the label is also a manufacturer under Part 111 and, under section 111.75, must qualify its supplier rather than rely on a Certificate of Analysis alone, confirming the COA with its own testing, documenting the qualification and reconfirming it periodically.
Can I get samples before committing?
Yes. For catalog formulations we can provide samples of the existing product so you can assess taste, texture and presentation before committing to a run. Samples of a modified formula take longer, because the modification has to be made first. Sample terms are confirmed together with your quote.
What drives the timeline on a private label project?
About 12 weeks from approved formula and packaging to finished goods. The formulation already exists, so the variable is almost always packaging component availability rather than manufacturing capacity — bottle, closure, carton and label lead times, plus your artwork approval and the production slot. One component out of stock is what moves the date.
Do you also make personal care products?
Yes. The same facility makes serums, creams, lotions, sprays and oils with a 5,000-unit minimum order quantity, so a brand launching a supplement and a companion topical uses one vendor, one quality system and one documentation package. See private label skin care manufacturing and serum manufacturing.
Do you white label?
No. We do not keep pre-made stock waiting for a label. Every lot is manufactured to order, so your product ships with its full shelf life and every repeat run matches the same specification.
Pick a formula. Put your brand on it.
Browse the catalog, tell us the format and the volume, and we will come back the same business day with whether it fits and what it takes. If it does not fit, we will say so rather than quote you into a corner.
BioB Manufacturing — the finished-goods arm of Bio-Botanica, Inc. NSF GMP, FSSC 22000, FDA-registered, 160,000 sq ft in Hauppauge, New York. Botanical extracts sourced globally and made in New York since 1972.