Fluoride & Anti-Cavity
Standard FDA-monograph compliant formulations, developed and documented for OTC sale in the markets you are shipping to.
Scalable, GMP-certified production for established oral care brands, dental professionals, and scaling startups. From custom R&D to turnkey private labeling.
Formulation Breadth
Six families cover almost every brief that reaches our laboratory. Each one has a validated base, a documented active system and a testing route behind it — so development starts from proven ground instead of a blank page. Raw materials are specified in our ingredient catalogue.
Standard FDA-monograph compliant formulations, developed and documented for OTC sale in the markets you are shipping to.
Clean-label builds using botanical ingredients, xylitol and hydroxyapatite (nHAp) for remineralisation without fluoride.
Peroxide-based, charcoal or enzyme-activated systems, balanced against a controlled RDA so whitening does not come at the cost of enamel.
Potassium nitrate or stannous fluoride formulations, with fluoride uptake and abrasivity work done before the claim goes on the carton.
Safe-to-swallow, low-abrasion formulas with custom flavours and age-appropriate active levels, produced to paediatric tolerance limits.
Herbal, Ayurvedic, vegan and probiotic toothpastes — including stability work on live cultures and plant extracts that behave differently in a paste base.
Service Models
Three routes into production, all running on the same equipment and the same quality system. Most brands start on one and move to another as volume grows.
For brands that want a proprietary formula nobody else can order. Our chemists work from your brief and your benchmark products.
Best for: established brands building a defensible product.
Fast-to-market, pre-tested base formulas that already carry stability data, ready for your branding and artwork.
Best for: fast launches, clinics, retail own-brand programmes.
You supply the bulk formula, we handle filling, sealing, coding and secondary packaging on qualified lines.
Best for: brands with an existing formula and no production asset.
Packaging & Filling
Format decides how the product is filled, shipped and merchandised. We run the common formats in-house and source the rest through qualified component partners.
ABL, PBL and aluminium bodies across a range of diameters and fill volumes, with matched caps and orifice sizes.
Airless dispensers for liquid-gel and serum textures, plus jars for tablet and powder formats.
Sugarcane-derived tubes, PCR plastic content and recyclable aluminium, specified with documentation to support the claim.
Cartoning, shrink wrapping, multi-pack bundling and retail-ready display trays packed to your retailer’s case specification.
Packaging is specified and compatibility tested alongside the formula, not after it — see the full breakdown on our custom toothpaste packaging page.
Quality & Compliance
Toothpaste — particularly fluoride and sensitivity products — is a regulated category. Our quality system is built so that the paperwork your regulator or retailer asks for already exists before anyone asks. Our QA/QC system is documented under compliance and quality.
Strict adherence to Current Good Manufacturing Practices, with documented batch records, cleaning validation and full raw-material traceability.
Registered OTC drug manufacturing for therapeutic products, which is what fluoride and anti-sensitivity toothpastes are classified as in the United States.
Assay, pH, viscosity, RDA and microbiological testing run on site, so results come back in days rather than through an external queue.
Accelerated and real-time stability programmes, with every batch held under QA release until testing results are signed off — nothing ships on assumption.
Certificates of analysis, stability summaries and regulatory documentation are issued with your order. Market-specific requirements are confirmed at briefing stage.
How We Work
A defined path from first call to delivered stock, with one named contact throughout. Here is what happens, in order.
01
Defining scope, MOQ and product requirements, plus the regulatory market and launch window you are working to.
02
Lab-scale formulation, flavor matching and sample approval — you test the prototypes before anything is committed to production.
03
Stability, microbial and pack-compatibility testing, with artwork checked against the regulations of the destination market.
04
Scaling up to full commercial runs, from pilot batches through to compounding, filling, sealing and coding.
05
Final batch testing and QA release, then palletising and global logistics to your warehouse or 3PL.
Why Us
Four practical reasons buyers stay with us past the first production run.
One partner from a 10,000-unit launch run through to multi-million unit annual programmes, without re-qualifying the formula.
Agile lead times and managed raw-material supply, so a formulation approval does not turn into a six-month wait for components.
A single point of contact who owns your project from brief to delivery — no relaying questions between departments.
True end-to-end service: raw material sourcing, formulation, filling, packing, documentation and final freight.
FAQ
Contract manufacturing runs start at 10,000 units for a custom printed tube and carton combination. Stock tubes with printed labels can start lower, which is usually the better route for a first market test.
MOQ depends on tube size, fill volume and how many SKUs are in the launch. Share your target volume and we will confirm the number that applies to your project — and tell you honestly if a smaller run makes more sense elsewhere.
Yes. Fluoride and anti-sensitivity toothpastes are OTC drug products in the United States, and we manufacture them in an FDA-registered facility under cGMP. That covers monograph-compliant active levels, fluoride release and uptake testing, and label artwork checked against FDA and FTC requirements.
Requirements differ by country, so we confirm the applicable standard for your destination market during the briefing — not after the formula is locked.
A new custom formulation typically takes three to six months from signed brief to production release. Prototyping and iteration occupy the first two to three months, and the balance is stability and regulatory testing that has to run in real time.
A private label route is considerably faster, since the base formula already carries stability data. We give you a written schedule before work starts, with packaging development often running in parallel with later testing.
Yes. We can supply sugarcane-derived PE tubes, laminate tubes with post-consumer recycled content, mono-material HDPE constructions designed for kerbside recycling, and FSC-certified cartons printed with soy-based inks.
Each option still goes through the same compatibility and seal testing as a conventional laminate, so a sustainability claim never comes at the expense of a stable product.
Private label toothpaste uses an existing or established formula that can be produced under your brand, making it a faster route to market. Custom manufacturing involves developing or modifying the formulation around your specific performance, ingredient, sensory or market requirements.
Private label is usually the better choice when speed and lower development cost are the priorities. Custom formulation is more appropriate when your product needs a differentiated formula or specific claims.
Yes. Custom toothpaste development can be built around your target market, product positioning, ingredient preferences, sensory profile, active ingredients and performance requirements.
The development process typically includes formulation, laboratory prototypes, evaluation and refinement before the final formula moves into stability, compatibility and regulatory testing.
Yes. We can support toothpaste projects with different formulation directions, including fluoride-free, natural-positioned and herbal products, subject to the ingredients, claims and regulatory requirements of the target market.
Our formulation team can review your ingredient brief and help determine which formulation approach is appropriate for the intended product claims and sales region.
Yes. Whitening, sensitivity-focused and other functional toothpaste products can be developed or manufactured according to the required formulation and target market regulations.
Because active ingredients and product claims can affect regulatory classification, testing and labeling, we review the intended claims and destination market before finalizing the formulation.
Yes. Laboratory and pilot samples can be produced during the development process so your team can evaluate texture, flavor, appearance, dispensing performance and other product characteristics before commercial production.
For a custom formulation, sample iterations may be required before the final formula is approved. A production sample can then be reviewed before the full manufacturing run.
Testing depends on the formulation, product claims and target market. Depending on the project, this can include stability testing, microbiological testing, packaging compatibility, active ingredient testing and other regulatory or product-performance evaluations.
The testing plan is established during development so required work can be completed before the commercial production release.
Once the formula, packaging, artwork and production specifications are approved, the manufacturing schedule depends on order quantity, packaging availability, SKU count and required quality testing.
We confirm the production and delivery schedule before the order is released so your purchasing and launch teams have a clear timeline from approved formula through finished goods.
Yes. Contract manufacturing can include bulk toothpaste production, tube filling, tube sealing, capping, coding, cartoning and final packing, depending on the project requirements.
This integrated approach allows formulation, filling and packaging specifications to be coordinated under one production schedule, reducing the need for separate suppliers.
Yes. International toothpaste projects can be developed around the regulatory, labeling and packaging requirements of the destination market.
During the initial briefing, we review the target country, product category, ingredients and intended claims so the formulation and packaging development can be aligned with the market requirements from the beginning.
Quality control can cover incoming raw materials, in-process production checks, finished-product testing, microbiological testing, fill weight, appearance, packaging integrity and batch documentation.
The exact quality plan depends on the product and regulatory requirements. Production specifications and acceptance criteria can be agreed before commercial manufacturing begins.
Yes. Multiple toothpaste SKUs can be planned within the same manufacturing program, subject to minimum quantities, formulation requirements, production capacity and packaging specifications for each SKU.
For a multi-SKU launch, we can review the volume and production sequence together to help reduce unnecessary changeovers and keep the overall launch schedule manageable.
We normally need your target market, product type, estimated annual or initial volume, desired fill size, formulation requirements, product claims and packaging preferences.
If you already have a formula, technical specification, artwork or packaging design, those documents can be reviewed during the initial project assessment. If you are starting from an idea, we can begin with a product brief and development requirements.
The cost of contract manufactured toothpaste depends on the formula, active ingredients, raw materials, fill size, order quantity, number of SKUs, packaging and testing requirements.
Custom formulation projects also include development and testing costs, while private label products can usually be quoted more directly because the formula is already established. Share your target volume and product specification for a project-specific quotation.