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Endo Relief Gummies

Private label endo relief gummies for supplement brands.

Endo Relief Gummies — product image
Endo Relief Gummies — doypack packaging
Endo Relief Gummies — Vitamin E ingredient reference
Endo Relief Gummies — gummies format detail
Price
Pricing confirmed on request
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.

PET bottle
From 1,000 units

The standard PET jar route for a first production run.

Order tiers
1,000 2,500 5,000 10,000 units
Doypack
From 2,500 units

Stand-up pouch packaging on the same private-label route.

Order tiers
2,500 5,000 10,000 units
Gummy sachet
From 1,000 units

Single-serving sachet — gummies portioned for daily-routine and travel.

Order tiers
1,000 2,500 5,000 10,000 25,000 units

Pricing confirmed on request — Request a quote.

Overview

Product overview

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

Endo Relief 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 Women's Health entry named for an audience, not a mechanism

Endo Relief Gummies is named for the audience and range concept it belongs to, and the formula table backs that with three tracked actives — curcuma longa turmeric, vitamin E (D-alpha-tocopherol) and boswellia — sitting together rather than one dominant ingredient carrying the name on its own.

Turmeric and boswellia are two botanicals that show up together across a number of catalogue formulas built around this kind of range concept, while vitamin E's role here reads as the standard antioxidant-adjacent cofactor pairing the catalogue uses elsewhere, rather than a second headline active in its own right. None of the three ingredients is exclusive to this range concept individually, but the specific three-ingredient combination is what the formula table ties to this SKU's name.

Where this sits in a Women's Health range

Catalogued under Women's Health, this SKU sits in the catalogue's women's-focused range family rather than in a general wellness or performance category — the audience the name targets is the same audience the category tag confirms.

A three-ingredient formula this specific is not a general-purpose range-filler: turmeric, boswellia and vitamin E together make this a distinct, purpose-built entry a brand adds when it wants a dedicated line item in a Women's Health range rather than a broad multivitamin extension. A brand launching into this category typically treats it as that dedicated line item rather than folding it into a broader wellness range, given how specifically the name targets its audience.

Personalising and ordering this formula

Make it Yours applies to this exact turmeric, boswellia and vitamin E formula — approved flavour, colour and shape only, with the three-ingredient composition held fixed. Product naming and label artwork run through the standard private-label branding process, separate from this step.

Any change to the actives, the amounts, or the claims made on pack moves the project into the separately scoped Custom Formula R&D route. Samples of this exact formula go out first, and the brand owner carries the label-claims and market-compliance review throughout — a name like this one is worth that extra care at the label stage.

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; % 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.

Try it first

Sample Endo Relief 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

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.

View how documentation works →

Start in portal →
  • Product specification
    Order gate

    Drafted at brief stage; locked before production. FDA/US market compliance confirmed.

  • Nutrition / supplement facts
    Order gate

    Per-serving values and the US Supplement Facts label (21 CFR 101.36). Prepared per target market and DSHEA framework.

  • Artwork checklist
    Order gate

    Dieline, on-pack copy and structure-function statement wording reviewed against DSHEA (21 USC §343(r)(6)) compliance.

  • Batch / release documents
    Order 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 dossier
    Order gate

    Supporting documentation (DSHEA structure-function substantiation, ingredient sourcing, FDA compliance evidence per 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 Endo Relief 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.

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 Endo Relief Gummies

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.