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Daily Multivitamin Powder

Private-label daily multivitamin powder (powder format).

Daily Multivitamin Powder — sachet format reference image
Daily Multivitamin Powder — Vitamin A ingredient reference
Daily Multivitamin Powder — Vitamin C (Ascorbic Acid) ingredient reference
Daily Multivitamin Powder — Vitamin E ingredient reference
From
€8.30/unit
at 10,000+ units · freight billed separately
MOQ
From 1,000 units
Lead time
From 8–12 weeks
Confirmed at order setup
  • 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
The Launch Loop
  1. 1 Select
  2. 2 Review
  3. 3 Sample
  4. 4 Approve
  5. 5 Produce
  6. 6 Deliver
Order options

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.

Powder sachet
From 1,000 units

Single-serving sachet for powders, granulates or compact daily-routine concepts.

Order tiers
1,000 2,500 5,000 10,000 25,000 units
From €8.30/unit
at 10,000+ units · freight billed separately
Overview

Product overview

The reviewed private-label concept, framed for brand owners.

Daily Multivitamin Powder is a private-label powder sachet delivering Vitamin A, Folate, Biotin per serving. Manufactured in the EU to GMP standards, additive-ready for your brand. Available for private label from MOQ 1,000 units with custom flavour, dosing and packaging.

Composition

Active ingredients

The actives in the current standard formulation. Final formula is reviewed and locked against the project brief.

Full composition (per-serving)

Per-serving dose; % NRV shown where an EU Reference Intake exists. Values reflect the current standard formulation and are locked at specification stage.

Try it first

Sample Daily Multivitamin Powder 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

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.

View how documentation works →

Start in portal →
  • Product specification
    Order gate

    Drafted at brief stage; locked before production. EU/EFTA market compliance confirmed.

  • Nutrition / supplement facts
    Order gate

    Per-serving values and the EU on-pack nutrition facts panel (Regulation 1169/2011). Prepared per target market.

  • Artwork checklist
    Order gate

    Dieline, on-pack copy and claim wording reviewed against EU 1924/2006 and the authorised list under Reg. 432/2012.

  • Batch / release documents
    Order gate

    Issued after production and QC release — always batch-scoped. EU GMP certification available on request per project scope.

  • Compliance dossier
    Order gate

    Supporting documentation (1924/2006 claim compliance, 432/2012 authority assessment, ingredient sourcing per market and project scope).

  • Certificate of Analysis
    Order 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.

Best fit for

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 Daily Multivitamin Powder into an existing supplement range as a powder sachet 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.

FAQ

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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Project handoff

Build a launch around Daily Multivitamin Powder

Start with this formula, order samples, or configure your production order in the DAT Supply portal.

Quick context request

Get manufacturing context

Drop your work email and a member of the DAT team will follow up with the right context for this concept. Order documents, certificates and pricing are released through the client workspace in the DAT portal.

You will receive a short confirmation email. Order documents (specification, batch-specific COA, packaging documents) are released through the client workspace in the DAT portal once a brief is in place.