Start with a product direction, not a finished formula
A new gummy range starts with a few decisions: who the product is for, where it will be sold, what ingredient direction you want and how you expect the finished pack to look. You do not need every answer before contacting us. Tell us which parts of the brief are fixed and which you want to explore.
Dio Bio is the website brand of Zhengzhou Di’ou Biotechnology Co., Ltd. Our team handles international B2B discussions about human and pet nutrition, private label, formulation, packaging and sourcing. For this page, keep the project specific to human probiotic gummies. A brand reference helps explain your direction; the formulation and pack for your own project are agreed separately.
Choose the scope that fits your brand
We distinguish putting your label on a suitable selected product from developing a new formulation. That distinction gives the first conversation a clear starting point: are you keeping a selected specification, or asking to change the ingredients, gummy base or other product characteristics?
Our published starting points are bottle-label customization from 50 bottles and custom formulation from 500 bottles. Confirm that the selected gummy, pack and requested changes fit the relevant route. These are general service starting points, not confirmation that every strain, formula or package is available at the same quantity.
If you want to compare both routes, ask us to identify what stays fixed, what needs development, what the proposed sample represents and which parts of the quotation need separate confirmation.
Bring the gummy and its label into the same discussion
For a probiotic gummy, the product brief should connect the microorganism identity with the serving and finished gummy. NIH ODS identifies probiotics by genus, species and strain, and describes CFU as an expression of viable microorganisms. Specify the microorganism and declaration your brand requires before comparing offers.
With Dio Bio, include the proposed strain direction if known, the CFU statement and its time point, gummies per serving, base ingredients, flavor preferences and ingredients you want excluded. If strain selection is still open, say so. Available ingredients, formulation feasibility and the evidence for the finished product need project-specific review.
Then add the physical product and pack: shape, size or unit-weight preference, bottle or other packaging direction, closure, label area and intended storage information. These decisions belong alongside the formula discussion because the sample, pack and artwork should describe the same proposed product.
Use the sample discussion to confirm the brand presentation
Our project approach brings product direction, sample scope and artwork into a coordinated discussion. Before reviewing a sample, identify its version and the features it is intended to demonstrate. A packaging sample and a formulated gummy sample answer different questions; agree the scope rather than assuming one confirms everything.
A useful approval record can include the sample or specification reference, agreed ingredient direction, serving basis, appearance, flavor or texture observations, pack details and the changes still open. The record below is a discussion tool, not evidence that a particular laboratory or stability test has already been completed.
| Decision | What to put in your Dio Bio brief |
|---|---|
| Formula direction | Requested microorganism identity or questions to review, full proposed base and exclusions. |
| Serving and CFU | Gummies per serving, proposed declaration, time point and supporting evidence needed. |
| Sample scope | What the sample represents, its version and the points you want evaluated. |
| Brand pack | Container, closure, artwork direction and label language. |
Review the evidence for the selected project
Tell us the actual destination country and the documents requested by your importer or label reviewer. We can discuss the relevant product specification, ingredient identities, proposed testing and batch documentation for the selected supply. Evidence supporting a viable-count declaration and storage or shelf-life statement must correspond to the finished gummy and package.
Our documentation discussion includes the holder and scope of available document copies. Facility or system documents and a product’s batch COA serve different purposes. We do not treat a general certificate as proof that a new gummy formula or every destination is covered.
Start your probiotic gummy project with Dio Bio
Send your destination, intended users, ingredient direction, estimated quantity and preferred pack. Add a draft label or reference specification you are entitled to use, and mark undecided details as open. We can then discuss the appropriate project route and the next information needed for review.
Our initial project response is within 48 hours. A completed quotation, confirmed strain supply, sample schedule and production or dispatch arrangements are agreed for the selected project. Use the product page to see the gummy decisions we discuss, or send your brief directly.
Sources and project scope
The technical background above draws on the official source below. Company service descriptions reflect Dio Bio’s current private label and formulation page and the corresponding product project page. Ingredient background is separate from the evidence for a selected finished product and batch. Identify your destination for the applicable product and label review.