China-Based Vitamin OEM · ODM · Private Label

Vitamin Contract Manufacturer for Custom & Private Label Supplements

Gensei Global manufactures custom and private label vitamin supplements for international nutrition brands. We translate single-vitamin, B-complex, D3+K2, and multivitamin-mineral concepts into compressed tablets, hard capsules, softgels, gummies, chewables, and powder blends—supported by stability engineering, pilot sampling, and turnkey retail packaging.

Active Vitamer Sourcing Overage & Stability Planning 6+ Commercial Dosage Forms
CollaGensei private label vitamin packaging with softgels, hard capsules, tablets, gummies, chewables and powder supplements
Multi-format manufacturing across solid dose, oil-filled softgel, confectionery gummy, and dry powder lines.
Six Core Dosage FormatsTablets, capsules, softgels, gummies, chewables, and powders
Transparent Format MOQsClear starting batch benchmarks by production line
Stability-First FormulationVitamer compatibility, moisture control, and assay verification

Final formulation specifications, overage targets, commercial quotations, and production schedules are confirmed per approved product brief.

01 · Vitamin Manufacturing Solutions

Choose the Right Manufacturing Route

Whether your brand has a locked-in Supplement Facts panel or an early product concept, we align active vitamin forms, daily serving size, dosage format, and destination-market compliance before production.

01 / OEM CONTRACT MANUFACTURING

Manufacture Your Formula

Submit your existing Bill of Materials (BOM), label claim targets, and excipient preferences. We audit vitamer grades, active loading feasibility, process compatibility, and assay methods.

02 / CUSTOM ODM FORMULATION

Develop a Vitamin Supplement

Engineer a custom single-vitamin or multivitamin formula around your target demographic, bioavailable nutrient forms, taste/swallowability goals, and optimal delivery format.

03 / PRIVATE LABEL

Prepare Your Branded Line

Select from established vitamin formulations and customize unit counts, bottle/blister/pouch packaging, flavor directions, and market-ready private label artwork.

02 · Vitamin Product Applications

Vitamin C, B-Complex, D3+K2 & Multivitamin Projects

Selecting the right chemical form (vitamer) and raw material grade determines tablet compressibility, capsule fill volume, oxidative stability, and label claims.

Multivitamin & Multimineral

Daily A-to-Z nutritional formulas balancing 15–25+ micronutrients. We use microencapsulated vitamins and chelated minerals (bisglycinates/citrates) to minimize cross-oxidation and control tablet/capsule size.

Vitamin C Formulas

High-load Ascorbic Acid, DC 97% direct-compression granules, buffered Sodium/Calcium Ascorbate, or Liposomal Vitamin C—engineered with acidity control for chewables, gummies, powders, and tablets.

Vitamin D3 & K2 Combinations

Lanolin or vegan lichen Cholecalciferol (D3) paired with microencapsulated all-trans MK-7 (K2) in MCT/olive oil softgels, dry-filled capsules, or stabilized micro-tablets.

Active B-Complex & B12

Standard or methylated B-vitamin complexes featuring Methylcobalamin / Cyanocobalamin (B12), Pyridoxal-5-Phosphate (P-5-P B6), 5-MTHF Folate, and D-Biotin with targeted odor and moisture barriers.

Fat-Soluble Vitamins A & E

Retinyl Palmitate, natural Beta-Carotene, and natural d-alpha Tocopheryl Acetate (oil for softgels) or d-alpha Tocopheryl Succinate (dry powder for two-piece capsules and tablets).

Condition-Specific Blends

Immune, prenatal, hair/skin/nails, energy, and bone-health formulas combining targeted vitamins with botanical extracts, amino acids, or coenzymes (CoQ10) around your target serving size.

03 · Vitamin Formulation Engineering

Vitamin Stability, Compatibility & Potency Planning

Vitamins vary widely in sensitivity to heat, humidity, oxygen, light, and pH. Our R&D team aligns raw material coatings, processing temperatures, and barrier packaging so your product meets label claims through shelf life.

HPLC vitamin potency assay and analytical stability testing in Gensei Global quality control laboratory
01 / INGREDIENT COMPATIBILITY

Vitamer & Mineral Isolation

Prevent transition metals (iron, copper, zinc) and alkaline excipients from accelerating the degradation of Vitamin C, B1, B12, and K2 (MK-7) by selecting coated or microencapsulated raw materials.

02 / OVERAGE CALIBRATION

Scientific Input Overages

Formulate appropriate manufacturing overages for heat- and moisture-sensitive vitamins (especially in cooked pectin gummies and compressed tablets) to account for processing and storage decay.

03 / BARRIER PROTECTION

Moisture, Oxygen & UV Control

Pair hygroscopic and light-sensitive formulas with aqueous film coatings, opaque softgel shells, amber PET/HDPE bottles, silica gel desiccants, or Alu-Alu / PVDC blister foils.

04 / DOSAGE SUITABILITY

Active Payload Matching

Match total milligram/microgram active weight to the right physical format—avoiding oversized tablets or under-dosed gummies by balancing serving counts and excipient ratios.

Target input overages, HPLC / Titration / ICP-MS analytical assay methods, and accelerated or real-time stability protocols are customized and documented for each approved formula.

04 · Vitamin Dosage Forms

Choose the Vitamin Format That Fits Your Product

Explore our dedicated dosage-form manufacturing pages below for detailed tooling options, shell/base choices, and line specifications.

ビタミン錠

High-load compressed, film-coated, and scored tablets ideal for A–Z multivitamins, high-dose Vitamin C, and calcium/D3 combinations.

Explore Tablet Manufacturing ↗

ビタミンカプセル

Two-piece hard capsules (#00 to #3) in bovine gelatin, vegan HPMC, or pullulan shells—well suited for B-complexes and clean-label blends.

Explore Capsule Manufacturing ↗

ビタミンソフトジェル

Hermetically sealed liquid/suspension softgels engineered for fat-soluble Vitamins A, D3, E, K2, and omega-vitamin combinations.

Explore Softgel Manufacturing ↗

ビタミン入りグミ

Pectin or gelatin vitamin gummies with calibrated flavor masking, acid/sugar balance, and thermal overage control for kids and adults.

Explore Gummy Manufacturing ↗

Chewable Vitamin Tablets

Direct-compression chewable wafers and shaped tablets with sweetening, flavor masking, and smooth mouthfeel for Vitamin C and multivitamins.

Explore Chewable Manufacturing ↗

ビタミンパウダー

Water-dispersible vitamin drink mixes, electrolyte-vitamin blends, and single-serve stick packs or canisters with controlled flow and taste.

Explore Powder Manufacturing ↗
05 · Commercial Planning

Vitamin Manufacturing MOQ, Sampling & Lead Times

Use these dosage-form production benchmarks to plan your launch volume and timeline. Exact commercial terms are confirmed based on active ingredients, tooling, and packaging configuration.

投与形態 Typical Starting MOQ Lab Sampling & Evaluation Indicative Bulk Schedule
Standard Tablets 100,000 tablets / SKU 2–3 weeks for standard samples using stocked tooling 6–8 weeks after material readiness and sample approval
チュアブル錠 100,000 tablets / SKU 2–3 weeks for flavor, sweetness, and texture trials 6–8 weeks after material readiness and sample approval
ハードカプセル 100,000 capsules / SKU 7–15 working days for feasibility and lab hand-fills 6–8 weeks after material readiness and sample approval
ソフトジェル 100,000 softgels / SKU 2–4 weeks for oil-fill and shell compatibility samples 6–8 weeks after material readiness and sample approval
ビタミン入りグミ Quoted by mold & piece weight (typically 150,000+ gummies / SKU) 2–3 weeks for pectin/gelatin base and flavor lab trials 6–8 weeks after formula, mold, and packaging sign-off
ビタミンパウダー 100 kg per formula / flavor 100–300 g trial blend; ~2 weeks preparation 4–6 weeks from deposit payment to China export port
Schedule & logistics scope: Tablet, capsule, softgel, and gummy timelines reflect production lead times after deposit receipt, raw material readiness, and packaging artwork approval. Powder lead times reference arrival at the designated China export port (FOB/EXW). International ocean/air freight, customs clearance, custom punch tooling, and specialty imported raw materials may extend overall project timelines.
06 · Manufacturing & Quality

From Vitamin Formula Review to Batch Release

Every commercial vitamin run follows a documented quality management plan covering raw material identity, blend uniformity, in-process physical checks, and finished batch verification.

01

Lock the Specification

Confirm active vitamer forms, label claims, input overages, excipient compliance, and packaging barrier specs.

02

Approve Lab Prototypes

Evaluate pilot samples for physical dimensions, disintegration, taste/odor, and sensory performance.

03

Manufacture & Pack

Execute GMP-controlled blending, tableting/encapsulation/depositing, metal detection, and retail bottling or blistering.

04

Assay & Release

Review finished batch analytical test results, microbiological clearance, and export documents prior to dispatch.

Vitamin-Specific QC Checkpoints

  • Incoming raw material identity and potency verification against supplier COAs.
  • Blend uniformity and dosage-unit weight variation, hardness, friability, and disintegration checks.
  • Finished-product vitamin assay verification (HPLC / Titration / ICP-MS per agreed test scope).
  • Water activity ($a_w$), loss on drying, and seal integrity testing to protect moisture-sensitive actives.
  • Total plate count, yeast & mold, 大腸菌, サルモネラ菌, and heavy metal (Pb, As, Cd, Hg) screening.

Standard Qualification & Batch Documents

  • Master Formula Record (MFR) & Finished Product Specification sheet.
  • Raw material COAs, allergen declarations, and BSE/TSE or Non-GMO statements.
  • Batch-specific Certificate of Analysis (COA) issued prior to shipment release.
  • Supplement Facts / Nutrition Facts composition data for destination-market label review.
  • Optional third-party lab testing (SGS, Eurofins, or Intertek) and stability studies upon request.
Quality Management & Compliance

ISO & Halal System Certificates

Review our quality management and food safety certifications below. Complete supplier qualification packages, ingredient COAs, and batch-specific test reports are provided during project onboarding.

ISO 22000 Food Safety ManagementView Certificate ↗ ISO 9001 Quality ManagementView Certificate ↗ Halal Compliance CertificateView Certificate ↗

Product-specific Halal coverage (such as bovine vs. vegan capsule/gummy bases) and export documentation are confirmed per approved formula.

07 · Buyer Questions

ビタミン受託製造に関するよくある質問

Direct answers for supplement brand owners, formulators, and sourcing teams.

Can Gensei manufacture vitamin supplements across different dosage forms?

Yes. Depending on active payload weight and ingredient stability, we manufacture vitamin formulas as compressed tablets, two-piece hard capsules (gelatin/HPMC/pullulan), oil-filled softgels, pectin/gelatin gummies, chewable tablets, effervescent tablets, and dry powder blends.

Can I transfer my existing multivitamin formula or Supplement Facts panel?

Yes. Send us your Bill of Materials (BOM) or Supplement Facts panel along with your target dosage form and serving size. Our R&D team reviews vitamer forms, excipient compatibility, and input overages before preparing pilot samples.

What is the MOQ for vitamin tablets, capsules, and softgels?

Our standard starting MOQ is 100,000 units per SKU for compressed tablets, chewable tablets, hard capsules, and softgels (for example, ~1,660 bottles at 60 counts per bottle). Custom tooling or specialty imported raw materials may have specific minimum requirements.

What are the MOQs for vitamin gummies and powder blends?

Powder vitamin blends start at 100 kg per formula and flavor (with 100–300 g lab samples). Vitamin gummy minimums depend on piece weight, pectin/gelatin base, and mold configuration—typically starting around 150,000+ gummies per SKU.

How do you handle vitamin degradation, potency overages, and shelf life?

We select stabilized or microencapsulated raw materials (such as microencapsulated MK-7 and coated Ascorbic Acid), isolate reactive minerals, calibrate scientific input overages for heat- or moisture-sensitive actives, and pair the product with appropriate barrier packaging.

How long do vitamin sampling and bulk production take?

Lab sampling typically takes 7–15 working days for hard capsules, 2–3 weeks for tablets, gummies, and powders, and 2–4 weeks for softgels. Commercial bulk production generally takes 6–8 weeks for solid dose/softgel/gummy runs and 4–6 weeks for powders after material readiness and approvals.

What details should I include to get an accurate vitamin manufacturing quote?

Share your target vitamin ingredients and dosages per serving (including preferred forms like Methylcobalamin or D3+K2), desired dosage form, estimated order quantity, packaging format (bottles, blisters, pouches, or sachets), and destination country.

08 · Start Your Vitamin Project

Request a Vitamin Contract Manufacturing Quote

Share your target vitamin formula and preferred dosage form. Our technical team will review active loading feasibility, sampling steps, and commercial pricing for your market.

  • Vitamin ingredient list, preferred vitamer forms, or Supplement Facts
  • Target potency per serving and preferred dosage format
  • Estimated order volume (bulk units or retail-packed bottles/pouches)
  • Packaging configuration and destination market
玄制グローバル工業株式会社

Vitamin Supplement OEM & Private Label Manufacturing

sales@collagensei.com

Send Your Vitamin Project Brief













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