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Chasteberry Supplement Manufacturer

Vitex Chasteberry Supplement Manufacturer

  • OEM & Private Label Available
  • MOQ from 3,000 finished units
  • Sample 7–15 days after spec confirmation
  • Mass production 4–6 weeks after sample approval
  • cGMP/ISO/HACCP/FSSC

Vitex Chasteberry Supplements Manufacturing Solutions

KS Nutripharma is a chasteberry supplement manufacturer for OEM, ODM, and private-label programs. We develop finished women’s wellness capsules, tablets, and powders using the Vitex agnus-castus (chasteberry) grade specified for that product — with batch COA release.

Comparable quotes start with a defined product specification. Start with the formula and format you want to sell. We then define the Vitex grade around that specification — marker and HPLC method included — and quote the finished unit.

Already have a Vitex CoA? Send it. We check species, fruit, marker, and method before quoting.

Already have a formula? Send Your BOM · Still deciding the specification? Get a Vitex Specification Recommendation · Comparing suppliers? Send Your Vitex COA

Project factWorking specifications (confirmed on the RFQ)
BotanicalChasteberry (Vitex agnus-castus L.), dried ripe fruit only. Not leaf, stem, or flower. Not V. negundo or Viticis Fructus.
Working gradesFruit powder (identity, no marker milligram). Ratio 4:1 or 10:1. Standardized extract: 0.5% agnuside HPLC or ≥0.10% casticin HPLC (Ph. Eur. dry-extract floor).
OrganicConventional is the default. Organic fruit powder or extract when required — state it on the first RFQ. It changes supply, price, and lead time. Organic certificate ships with the lot.
Formula architecturesF01 extract capsule · F02 fruit-powder capsule · F03 B6 + magnesium · F04 dong quai · F05 evening primrose oil · F06 black cohosh · F07 maca · F08 myo-inositol
Recommended formatCapsules first. Tablets when minerals drive fill. Powder/stick for gram-class servings. Softgel only with an oil fill. Gummies and liquids after feasibility.
Serving & fill weightF01 extract: typically tens of mg per capsule. F02 fruit powder: hundreds of mg (often two capsules). F08 inositol: gram-class stick or split serving. 20 mg of 0.5% agnuside extract = 0.1 mg agnuside, not 20 mg agnuside.
Assay/releaseHPLC for named markers on standardized grades. Incoming identity, moisture, microbiology, and heavy metals. Finished SKU assayed against the same specifications used for the sample.
DocumentsBatch COA, specification sheet, SDS, allergen statement. Organic certificate when the SKU is organic. Halal / Kosher files when required. Third-party testing (SGS / Eurofins) on request.
MOQCapsules ~3,000–5,000 units · tablets ~5,000–10,000 · sticks often from ~10,000. Bulk powder/extract quoted by kg on a separate PO.
Lead timeSample 7–15 days after specification lock · commercial production 30–45 days after sample approval. Gummies, new flavored powders, and liquids take longer.
ProgramOEM / ODM / private-label finished SKUs. Bulk ingredient is a different PO, pack, and release file.

cGMP | ISO 9001 | ISO 22000 | HACCP | FSSC 22000 | Halal | Kosher | In-house lab + third-party pathways (SGS / Eurofins) | Batch COA | Traceable release

-> About Us | Manufacturing Capacity | Certifications | Quality Control

What you receive with a chasteberry OEM project

  • Matched raw-material specification
  • Formula and dosage-form feasibility review
  • Sample based on the approved specification
  • Prototype COA
  • Production quotation by SKU
  • Batch release documentation
  • Packaging and export support
Read More

Typical Chasteberry Formula Architectures We Manufacture

These eight briefs are the commercial patterns we quote most often. Each line is a formula architecture — Vitex grade plus partners plus format — until you lock the BOM.

F01 · Standardized extract capsule

Positioning: Compact Vitex-forward SKU on a named HPLC marker.

Format & spec: [Hard capsule](https://kssupplements.com/hard-capsules/). Lock 0.5% agnuside HPLC or ≥0.10% casticin HPLC, method ID, fill weight, and capsule size.

Manufacturing watch-out: Marker milligrams follow extract milligrams × % — confirm that math before artwork.

F02 — Whole-Fruit Powder Capsule

Positioning: Whole-fruit Vitex when the brief is botanical identity, not a marker milligram.

Format & spec: Capsules; two-count when fill is high. Lock mesh, moisture, and identity method (macro / TLC / HPTLC as specified).

Manufacturing watch-out: Do not print agnuside or casticin milligrams from fruit powder unless you add a standardized extract.

F03 · Extract + B6 + magnesium

F03 · Extract + B6 + magnesium

Positioning: Vitex with B6 and magnesium on a [women’s wellness stack](https://kssupplements.com/womens-hormone-balance-supplements/) that already carries those vitamins and minerals.

Format & spec: [Tablet](https://kssupplements.com/tablets/) when magnesium salt drives fill; two-count capsule if the brief stays HPMC. Lock salt, B6 form, Vitex grade, and compression.

Manufacturing watch-out: One-capsule briefs often fail fill or hardness; split serving or change salt before tooling.

F04 · Extract + dong quai

Positioning: Two-botanical women’s SKU. Each herb needs its own identity and grade.

Format & spec: Capsules. Lock Angelica sinensis root (not leaf), extract type, and Vitex marker if you claim milligrams.

Manufacturing watch-out: Two ratio extracts in one capsule are two different materials — quote each COA line.

F05 · Extract + evening primrose oil

Positioning: Vitex plus oil-soluble GLA. Softgel is a different formula from a dry-extract capsule.

Format & spec: [Softgel](https://kssupplements.com/softgel/) with EPO in the fill, or two SKUs (capsule + oil). Lock GLA %, shell type, and Vitex grade (oil-dispersible if one fill).

Manufacturing watch-out: Dry fruit powder or hydroalcoholic extract does not drop into an EPO fill without a new specification.

F06 · Extract + black cohosh

Positioning: Two-botanical SKU next to a [menopause assortment](https://kssupplements.com/menopause-supplements/). Black cohosh is a separate identity and claim-risk file.

Format & spec: Capsules. Lock Actaea racemosa / Cimicifuga racemosa root/rhizome, extract ratio or triterpene glycosides, and Vitex marker.

Manufacturing watch-out: Destination-market warnings for black cohosh stay on the brand’s label brief. We manufacture to the locked specification.

Choose the Chasteberry Format: Capsules, Tablets, Powder or Liquid

Match load, taste, moisture, serving size, and unit cost to the format after the formula architecture is chosen. Chasteberry is not equally straightforward in every dosage form.

  • Chasteberry Capsules

    Fastest start for F01, F02, F04, F06, and F07. A chasteberry capsule manufacturer path is usually the shortest RFQ when the formula is dry powder or extract.

    Best for: Standardized extract, fruit powder, two-botanical dry blends.

    Why: HPMC or gelatin, no compression curve, taste in the shell.

    Typical formula cards: F01, F02, F04, F06, F07. F03 if the brief stays two-count capsule. F08 only as a split serving.

    What to lock: Fill weight, capsule size, shell type, flow aid. Capsule size follows fill weight.

    Manufacturing note: High fruit-powder fill often means two capsules. Confirm bulk density on the RFQ.

  • Chasteberry Tablets

    Use when magnesium or other minerals make a one-count capsule unrealistic.

    Best for: F03 and other mineral-heavy stacks.

    Why: Higher payload per unit than a two-piece capsule of the same outline.

    Typical formula cards: F03 first. Extract-only F01 if the brand wants a small round tablet.

    What to lock: Compression, hardness, disintegration, coating, score.

    Manufacturing note: Fruit powder plus magnesium needs a compression trial. We do not promise a tablet from a capsule BOM without that trial.

  • Powder / stick packs

    Correct unit for gram-class inositol (F08). A stick is its own SKU — flavor, fill weight, and film — not a capsule formula poured into a sachet.

    Best for: F08; drink-style Vitex only when the brief accepts taste and sedimentation.

    Why: 2–4 g inositol does not fit a standard capsule.

    Typical formula cards: F08. Fruit-powder drink mixes as a separate RFQ.

    What to lock: Mesh, carrier, flavor, stick film, moisture spec.

    Manufacturing note: Hydroalcoholic Vitex extract can taste bitter. Flavor and sweetener are formula lines.

  • Chasterberry Gummies

    Feasible after a pectin/gelatin, pH, and taste trial. Heat and moisture in the cook can move markers — lock the assay on the finished gummy, not only on incoming extract.

    Best for: Compact extract milligrams when the brand accepts a longer development cycle.

    Why: Retail format. Not the default Vitex path.

    Typical formula cards: F01-type extract milligrams only. F08 inositol gummies need a separate sugar-alcohol / load review.

    What to lock: Gelling system, cook temperature, assay on finished piece, pack.

    Manufacturing note: Fruit powder at F02 loads is usually a poor gummy fill. Prefer standardized extract milligrams.

  • Chasteberry Softgels

    Use when the fill is oil (F05). Dry Vitex in a two-piece capsule is a different SKU from Vitex in an EPO fill.

    Best for: Evening primrose / GLA with Vitex in one unit, or dual-SKU programs.

    Why: Oil-soluble partners belong in a lipid fill.

    Typical formula cards: F05. Other cards stay capsules or tablets unless you add an oil phase.

    What to lock: Oil identity, GLA %, shell (gelatin vs vegetarian), leak test, Vitex grade in oil.

    Manufacturing note: If the brief is dry extract only, quote capsules. Softgel starts when an oil is on the BOM.

  • Liquid/liposomal

    Project-scoped. Solubility, preservative system, and assay on the bottled liquid are the gates. Quote liquids as a development brief, not as a pour-over from the powder formula.

    Best for: Brands that already sell liquids and can fund a stability protocol.

    Why: Different pack, different microbial and assay file.

    Typical formula cards: None of F01–F08 as written. Convert milligrams to a liquid brief on the RFQ.

    What to lock: Vehicle, preservative, pH, light protection, finished assay method.

    Manufacturing note: Liposomal claims need a defined process and test plan. We quote that as a development project.

Chasteberry Fruit Powder vs Extract vs Standardized Extract

“Chasteberry extract” is not a complete specification. Fruit powder, a 10:1 ratio extract, and a 0.5% agnuside extract are different commercial grades. A low $/kg quote is a different product — not a saving. For a meaningful cost comparison, calculate cost per finished serving against the same marker specification and method.

Grade

What you are buyingTypical use on this page

Quote / label implication

Fruit powderMilled dried ripe fruit. Identity and contaminants. No guaranteed marker milligram.F02; high-fill capsulesDo not print agnuside or casticin mg unless you add a standardized extract.
Ratio extract (4:1, 10:1)Process concentration (DER). Solvent and carrier still vary lot to lot.Compact fill when the brief is ratio, not % markerA 10:1 ratio does not mean 10× casticin or agnuside. Two 10:1 lots can still differ in HPLC.
Marker-standardized extractNamed % (e.g. 0.5% agnuside HPLC or ≥0.10% casticin HPLC) plus method IDF01, F03–F07 extract milligramsMarker mg = extract mg × %. Method must match the COA.
Powder + extract blendFruit identity plus a defined marker contributionHybrid SKUsLock both lines on the BOM.

Standard extracts are quoted with DER, solvent, carrier, and — when you need milligrams on pack — a named HPLC marker. Send the grade you want matched, or ask us to recommend one from F01–F08.

Send Your Vitex Grade / COA

Chasteberry Extract Specification, HPLC Markers, and COA

Lock species, plant part, extract type, marker, and method on the RFQ. Incoming lots, samples, and finished SKUs use that same lock.

Pharmacopoeial reference (fruit and dry extract)

These figures are pharmacopoeial reference limits. Confirm the current monograph text in your QA file; pharmacopoeias are revised over time.

ReferenceWhat it specifiesFigure
Ph. Eur. monograph 2147 Agnus castus fruitDried ripe fruit, casticinMinimum 0.08% casticin (dried drug)
Ph. Eur. monograph 2309 Agnus castus fruit dry extractDry extract, casticinMinimum 0.10% casticin (dried extract)
USP–NF Chaste Tree (fruit)Dried ripe fruitNLT 0.05% agnuside and NLT 0.08% casticin (dried basis)

Public citations: the EMA HMPC assessment report quotes Ph. Eur. 01/2015:2147 and 2309; the USP–NF Chaste Tree definition states the fruit NLT figures (full method text is subscription). USP Powdered Chaste Tree Extract is a labeled-amount monograph (typically 90.0–110.0% of labeled casticin and agnuside), which is not the same as the Ph. Eur. 0.10% casticin floor. Dietary-supplement SKUs may still purchase a tighter commercial marker (for example 0.5% agnuside HPLC) — that is a purchase specification.

DER, solvent, and carrier

DER is process concentration. After you pick 4:1 or 10:1, still lock solvent, native vs added carrier, and particle size — two 10:1 extracts remain different materials until those fields match.

Marker and HPLC method

A number without a method is not comparable. State agnuside or casticin (or both), %, and HPLC method ID. Incoming COA, sample, and finished SKU must use the same trio.

COA checklist (incoming extract or powder)

Botanical identity · plant part · extract type / DER · marker % and method · loss on drying · particle size / bulk density (for fill) · residual solvents (extracts) · heavy metals · pesticides · microbiology · carrier declaration. Organic lots: organic certificate on the same shipment.

Request the Specification Sheet

Chasteberry Serving Size Follows Extract Grade and Fill Weight

Serving follows formula architecture plus the locked raw-material specification. The arithmetic below is illustration only, not a dose recommendation.

ExampleArithmeticWhat the label can honestly support
20 mg extract × 0.5% agnuside20 × 0.005 = 0.1 mg agnuside0.1 mg agnuside, if the method matches
20 mg extract × 0.5% is not 20 mg agnusideDo not print extract milligrams as marker milligrams
Fruit powder 400 mgNo guaranteed marker mgIdentity / weight only unless a standardized line is added

One EU well-established-use herbal-medicine preparation in the EMA HMPC monograph on Vitex agnus-castus L., fructus is a specific 20 mg dry extract (DER 6–12:1, extraction solvent ethanol 60% m/m), once daily, under that herbal-medicine classification. That is a medicinal pathway in the EU file — copy it onto a U.S. dietary-supplement serving only with a destination-market brief.

Capsule size follows fill weight. F02 fruit powder often needs two capsules. F08 inositol at 2–4 g belongs in a stick or a split serving.

Confirm Serving Math on Your Spec

Manufacturing Challenges We Solve for Chasteberry Supplements

Approving the raw-material specification is step one. The points below belong in the sample plan, so the SKU can run at scale.

Botanical identity and lot consistency

Near-related Vitex fruits can enter the supply chain. The sample plan should confirm species, plant part, and the fingerprint method scoped on the approved file — plus marker, moisture, and microbiology on the same lot used for the sample.

Release method: UV total vs HPLC marker

A brief that asks for an HPLC marker and a supplier file that only states a ratio or a UV flavonoid total are different offers. Samples can still look acceptable. Commercial lots then fail when the release method is the one written into the specification. Align marker and method before comparing price.

Capsule fill, magnesium salt, and tablet compression

F02 fruit powder and F07 maca consume capsule volume. F01 extract milligrams usually do not — until F03 magnesium or F04/F06 botanicals are added. Oxide and glycinate magnesium are different fills. F08 inositol is gram-class: quote powder/stick or a split serving. Flow aids, granulation, hardness, or a format change are decided at sample.

Taste and open formats

Chasteberry extract is often bitter and pepper-like. Capsules isolate that. Gummies, flavored powders, sticks, and liquids do not. Taste masking adds excipient load and sample time. Gummy cook also adds heat and water activity — assay the finished piece.

Moisture, pack, and shelf life

Stability evaluation should consider moisture, light, and oxygen for casticin- and agnuside-bearing extracts. Film coating, desiccant, and higher-barrier pack are evaluated against the formula, the dating target, and distribution climate. A stability protocol is scoped when dating is claimed. Raw-material shelf life does not establish finished-product dating.

Multi-ingredient compatibility

Co-ingredientArchitectureWhat to check on the BOM
Vitamin B6F03Salt form, fill contribution, destination-market serving limits
MagnesiumF03Salt form vs capsule/tablet size; hygroscopicity and compression
Dong quaiF04Separate identity, assay, and claim-risk file
Black cohoshF06Species, triterpene specification, destination safety file
Evening primrose oilF05Oil on the BOM: softgel or dual SKU
MacaF07Powder vs extract grade, origin claims, fill budget
Myo-inositolF08Gram-class serving; powder/stick vs split capsules
Flavored powders / gummiesCustomCombined bitterness; masking load; heat and water activity

Open formats add sensory and stability work to the sample. With an agreed barrier pack, capsules remain the shortest path to a dated SKU.

Ask for a Feasibility Review

Quality Control from Incoming Vitex to Batch Release

Control path: Specification lock → Incoming QC → In-process checks → Finished QC → QA release. Each node is a pass / hold / reject decision against the same specification.

StageWhat we decide
SpecificationSpecies, fruit, grade, marker, method, format, pack — signed before sample.
Incoming QCIdentity, marker (standardized lots), moisture, micro, metals, solvents, pesticides as specified. Hold if the COA does not match the lock.
In-processBlend uniformity, fill weight, hardness / leak (format-specific).
Finished QCAssay vs the same marker/method; micro; pack integrity.
QA releaseBatch COA, retain sample, traceable lot file. Shipment only after release.

In-house lab plus SGS / Eurofins when the RFQ requires a third-party report. Quality control is the same path for other botanicals; Vitex adds fruit-only identity and the named HPLC pair.

Request a Sample COA Template

Chasteberry Supplements Regulatory Notes for US, EU, UK, AU and Canada

KS Nutripharma manufactures to the locked specification and supplies the documentation pack. Brand owners own the finished label with local counsel.

  • United States: Dietary supplement. Structure/function copy and DSHEA notification (if used) are the brand’s file. Vitex traditional-use language is not a disease claim.
  • EU / UK: Food supplement vs herbal-medicine pathways differ. The EMA HMPC well-established-use extract above is a medicinal classification in that monograph — do not paste it onto a food-supplement label without a regulatory brief.
  • Australia / Canada: Listed / NHP style files need the exact herb, part, and extract as registered. We match the manufacturing spec; we do not file the listing for you unless contracted.

F06 black cohosh and F08 inositol may carry extra destination warnings or claim limits. Flag the market on the first RFQ.

Send Your Destination Market

OEM, ODM and Private Label Process for a Chasteberry SKU
  1. Brief — Formula architecture (or BOM), format, market, organic vs conventional.
  2. Specification — Vitex grade, partners, fill, pack, test plan.
  3. Sample — Manufactured against that specification.
  4. Approval — Artwork and COA alignment.
  5. Production — Commercial batch.
  6. Release — QA batch file, then shipment.

R&D supports specification and sample. Manufacturing capacity covers the format you lock. Processing technologies apply when extraction or granulation is on the brief.

Start the Specification Brief

Chasteberry Supplement Factory MOQ & Lead Time by Format

MOQ and lead time depend on dosage form, formula complexity, packaging, testing, material availability, and production scheduling.

FormatTypical MOQ (guide)SampleCommercial production after sample approval
Capsules~3,000–5,000 units7–15 days after spec lock~30–45 days
Tablets~5,000–10,000 units7–15 days after spec lock~30–45 days
Powder / stickOften from ~10,000 sticks (or kg-based bulk fill)Longer when flavor is newOften longer than capsules
GummiesProject quoteDevelopment + sampleLonger cook / set / assay cycle
SoftgelsProject quote (oil fill)After oil + shell lockPer oil-fill calendar
LiquidsProject quoteAfter preservative / assay lockPer liquid calendar

Bulk powder or extract, when ordered as ingredient, is a separate kg PO with a different pack and release file from the finished SKU.

Organic fruit or extract, new flavor systems, and third-party (SGS / Eurofins) panels add time. Confirm the window on the RFQ.

Get MOQ and Lead Time for Your Format

Bulk Chasteberry vs Finished Supplement Manufacturing

We quote finished capsules, tablets, powders, and (when feasible) gummies, softgels, and liquids. Bulk fruit powder or extract is available on a separate PO when you need kg for your own plant.

Same botanical, different program: finished SKU includes formula, format, pack, and batch release. Bulk is identity + spec + kg. Do not compare a bulk $/kg line to a bottled-unit quote.

Ask Which PO You Need

Get a Chasteberry Supplement Manufacturer Quote

A vague “chasteberry capsules” request is not an RFQ — the quotes you get back will not be comparable. Tell us the selling market, the closest formula architecture (or your BOM), and the format. Fruit powder versus extract, marker specification, and method follow that brief. If the formula is still open, say so.

You do not need a finished formula to start. A market, a formula direction, and a format are enough. If you already have a COA or a BOM, send that instead — we check whether you are pricing the same Vitex grade before you spend a sampling cycle.

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