Ashwagandha Gummies
Ashwagandha Gummies is a private-label pectin-gummy supplement concept for brands building a daily wellness range.
- 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
Available for private-label production. Samples available before production.
- 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.
Product overview
The reviewed private-label concept, framed for brand owners. Final claims, documentation and market suitability are reviewed per target market and project scope.
Ashwagandha Gummies is a private-label gummy SKU available for brand launches. Manufactured in Europe 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.
Final claims, documentation and market suitability are reviewed per target market and project scope.
Active ingredients
The actives in the current standard formulation. Final formula is reviewed and locked against the project brief.
- Withania Somnifera Root Extract
- Vitamin B6 (Pyridoxine) Pyridoxine — a workhorse of B-complex and women's health stacks. View ingredient →
Per-serving dose; % NRV shown where an EU Reference Intake exists. Values reflect the current standard formulation and are locked at specification stage.
- Withania Somnifera Root Extract 300 mg
- Pyridoxine Hydrochloride 2.8 mg
Sample Ashwagandha 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 (EU 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. EU/EFTA market compliance confirmed.
- Nutrition / supplement factsOrder gate
Per-serving values and the EU on-pack nutrition facts panel (Regulation 1169/2011). Prepared per target market.
- Artwork checklistOrder gate
Dieline, on-pack copy and claim wording reviewed against EU 1924/2006 and the authorised list under Reg. 432/2012.
- Batch / release documentsOrder gate
Issued after production and QC release — always batch-scoped. EU GMP certification available on request per project scope.
- Compliance dossierOrder gate
Supporting documentation (1924/2006 claim compliance, 432/2012 authority assessment, ingredient sourcing per market and 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 Ashwagandha 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 EU regulation 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 5–12 weeks depending on format, packaging, production slot and destination. Final timeline is confirmed during order setup before payment.
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