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Vitamin E Drops

Private-label 30 mL dropper bottle, 1 mL serving, 30 servings.

Vitamin E Drops — liquid drop reference image
Vitamin E Drops — Vitamin E ingredient reference
Vitamin E Drops — Beauty & Skin category visual
Vitamin E Drops — liquid drops format detail
From
€3.30/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.

Dropper bottle
From 1,000 units

Dropper-bottle format for oil-soluble or precise-dose actives.

Order tiers
1,000 2,500 5,000 10,000 units
From €3.30/unit
at 10,000+ units · freight billed separately
Overview

Product overview

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

A single-active liquid alternative to a softgel

Vitamin E Drops is a single-active liquid formula built on d-alpha-tocopherol, delivered through a dropper bottle rather than a capsule or gummy. A liquid vitamin E format is less common in the wider market than a softgel capsule, giving a brand a distinct pack format for a well-recognised ingredient that most competitors still sell in capsule form. The distinction is worth carrying into any listing copy or pack description a brand drafts from this catalogue record. A brand reviewing the record should treat this as the working formulation reference for any pack copy it drafts from scratch.

The dropper format is the same delivery mechanism the catalogue uses for its other single-active drop SKUs, so a brand adding this alongside a companion drop, biotin, for instance, can offer a consistent bottle-and-dropper experience across a small liquid-format sub-range rather than mixing delivery mechanisms across its beauty listings. A brand should rely on the confirmed record, not the product name alone, as the reference point for its own listing copy. This is the kind of detail a brand's own quality or regulatory reviewer would expect to see carried through consistently.

The simple, ingredient-led liquid tier of beauty

Beauty & Skin is the catalogue's range for beauty brands and subscription boxes building hair, skin and nail-led concepts, and a single-active liquid vitamin E like this one sits in the simple, ingredient-recognisable tier of that range, next to the more complex multi-active beauty gummies and jellies rather than replacing them. Where a brand positions this SKU relative to its other listings is ultimately a range-planning decision made during order setup, not a fixed rule. A brand mapping its own range against the catalogue's category structure would place this SKU accordingly before adding further concepts around it over time.

Biotin Beauty Drops is the closest same-format sibling in the same category, and Antioxidant Complex Gummies and CoQ10 Radiance Gummies are the confirmed vitamin-E-containing gummy siblings, pairing the same active with CoQ10 in a chewable format instead of a liquid one. These comparisons are a planning aid, not a fixed hierarchy the brand's own range has to follow. A brand building out a fuller range would typically revisit this placement as more SKUs are added alongside it and shopper feedback comes in. This positioning is a reasonable starting point rather than a fixed placement, and a brand can weight it differently once its own range takes shape.

Personalising and ordering this single-active formula

Make it Yours covers approved flavour, colour and shape on this single-active formula. On a liquid drop, flavour and bottle presentation carry more of the differentiation weight than they would on a chewable format, since the bottle is most of what a shopper actually sees before buying. A brand should raise any pack-presentation preference at this stage rather than after artwork is already underway and harder to change. Artwork and packaging presentation are typically reviewed alongside flavour during the same personalisation step, rather than as a separate pass.

Adding a second active, changing the vitamin E dose, or introducing a new beauty-related claim moves the project into the separately scoped Custom Product R&D route instead. Sampling this exact formula comes first, and label claims plus market compliance remain the brand owner's responsibility throughout the ordering process. These decisions are typically locked before a sample is produced, rather than revisited afterward. A brand's own branding team usually leads this step, with DAT Supply confirming what the fixed formula and format allow. This step is where a brand's own branding decisions and the catalogue's fixed formula meet, ahead of sampling and any production commitment.

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.

Active ingredients
Try it first

Sample Vitamin E Drops 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 Vitamin E Drops into an existing supplement range as a drops 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 Vitamin E Drops

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.