- Private-label formula ready for your brand
- Order samples before production
- Choose PET bottle or doypack during order setup
- Documents and approvals managed in the portal
- 1 Select
- 2 Review
- 3 Sample
- 4 Approve
- 5 Produce
- 6 Deliver
Packaging and minimum order quantities
Confirmed against your brief during order setup — after you have seen samples, never before. Project-specific packaging, flavour, colour or shape adjustments may be reviewed after order start.
The standard PET jar route for a first production run.
Stand-up pouch packaging on the same private-label route.
Single-serving sachet — gummies portioned for daily-routine and travel.
Product overview
The reviewed private-label concept, framed for brand owners.
Folic Acid Gummies is a private-label gummy SKU available for private-label brand launches. manufactured to specification under EU food supplement directives. Pectin-based formulation by default. Standard MOQ is 1000 units (HDPE jar) or 2500 units (doypack). Custom packaging and formulation development available subject to MOQ tier. Documentation pack included for the target market's notification regime.
A folic-acid-named gummy confirming vitamin B12 in its formula table
Folic Acid Gummies carries the Women's Health range's folate-adjacent naming, though the row's itemized formula lists cyanocobalamin — vitamin B12 — as the confirmed dosed active, a common pairing partner for folate rather than folate itself. A brand should regard the B12 entry as the confirmed fact and the folic-acid name as the catalogue's stated positioning.
It is manufactured as a pectin-based gummy under EU food supplement rules, the same default gummy platform the rest of the catalogue's gummy SKUs share, distinct from the jelly, powder or drop formats used for related Women's Health concepts.
Where a folate-named gummy sits in a Women's Health range
Within its own catalogue neighbourhood this gummy sits alongside Iron + C Jelly, Iron Drops and Iron Powder, each a confirmed iron-forward Women's Health concept in a different format, and Folate Drops, which carries the same folate name in dropper-bottle form with its own formula table still pending.
As the only gummy-format SKU among that group, it gives a brand a chewable option where the rest of the nearby range runs jelly, powder or drops instead. That format gap is itself a reason a brand might stock this gummy specifically, independent of how the folic-acid-versus-B12 naming question eventually resolves.
Personalising and ordering the Folic Acid Gummies formula
Make it Yours covers approved flavour, colour and shape on this exact formula — project-specific personalisation, not a formula change. On a single-active gummy there is no second ingredient competing for label space, so pack presentation and shape carry more of the brand-differentiation weight.
Confirming folic acid within the structured formula table, changing the active, or introducing a new claim moves the project into the separately scoped Custom Product R&D route instead. Samples of this exact formula come first, and label claims plus market compliance remain the brand owner's responsibility throughout.
Active ingredients
The actives in the current standard formulation. Final formula is reviewed and locked against the project brief.
Per-serving dose; % Daily Value (DV) shown for applicable nutrients per FDA 21 CFR 101.36. Values reflect the current standard formulation and are locked at specification stage.
- Vitamin B12 (Cyanocobalamin) 0.01 mg 400% % DV
Sample Folic Acid Gummies before you commit
Order a sample kit from your client workspace to review texture, flavour and finish — the expected next step before a production run.
Documents managed by order stage (US market)
Each document is released into your client workspace as the order moves through its review stages — never a public download. DAT releases the standard documentation package by project stage. External testing, full COA, additional microbiological reports, heavy metals, pesticide residue reports or raw-material supplier documentation are reviewed and quoted separately unless included in the agreed project scope.
- Product specificationOrder gate
Drafted at brief stage; locked before production. FDA/US market compliance confirmed.
- Nutrition / supplement factsOrder gate
Per-serving values and the US Supplement Facts label (21 CFR 101.36). Prepared per target market and DSHEA framework.
- Artwork checklistOrder gate
Dieline, on-pack copy and structure-function statement wording reviewed against DSHEA (21 USC §343(r)(6)) compliance.
- Batch / release documentsOrder gate
Issued after production and QC release — always batch-scoped. subject to per-market regulatory review testing summary available on request per project scope.
- Compliance dossierOrder gate
Supporting documentation (DSHEA structure-function substantiation, ingredient sourcing, FDA compliance evidence per project scope).
- Certificate of AnalysisOrder gate
A batch-specific Certificate of Analysis is available on request after production — ingredient identity, potency and contaminant screening.
Documentation availability depends on product, target market and project stage. The brand owner remains the food business operator and is responsible for final filings.
Where this concept sits
Where this concept slots into a brand plan. Positioning and claims are reviewed per project and target market.
Brand range expansion
Slot Folic Acid Gummies into an existing supplement range as the gummy SKU, with shared brand artwork direction and a per-SKU specification.
Adult daily-routine positioning
Pack copy positioned as part of an adult daily routine, with claim wording reviewed against target-market regulations per market.
Frequently asked questions
Can I request a sample before placing an order?
Yes. Sample requests go through the quote form. Lead time and sample format depend on packaging and any custom flavour or colour work.What is the MOQ?
MOQ is confirmed per project. Ready private-label option starts at 1,000 units in PET jars and 2,500 units in doypacks; custom configurations are confirmed after scope.Which markets is this product suitable for?
Market eligibility depends on the labelling, claims and certifications required for your destination — reviewed per project against the relevant EU / UK / non-EU framework.Do you provide a Certificate of Analysis?
A batch-specific Certificate of Analysis is provided after production and QC release. COA scope (microbiological, heavy metals, actives) is agreed up-front in the spec sheet.Can the formula be customised?
Common adjustments include flavour, colour, sugar profile and packaging count. Active-ingredient changes are evaluated against EU food-supplement rules and may move the SKU into a custom-formula tier.How long are typical lead times?
Lead time is typically 8–12 weeks depending on format, packaging, production slot and destination. Final timeline is confirmed during order setup before payment.
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