FDA 21 CFR Part 111 cGMP · Bilateral NDA Protected · ISO 22000

Turnkey Private Label Supplement Manufacturing & Bespoke OEM Contract Formulation

Engineered for agility and enterprise scale. Launch fast with 300+ proven, turnkey stock formulas at flexible low MOQs, or engineer proprietary, patent-protected custom nutraceuticals backed by our cGMP laboratory and strict intellectual property covenants.

In-House HPLC Potency TestingFull Heavy Metal & Microbial COA50+ Global Export Markets Cleared
Turnkey Dosage Ecosystem
9 Dosage Forms
Comprehensive Turnkey Private Label Supplement Bottling & Contract Manufacturing
Bilateral NDA•Class 100k Cleanroom•cGMP Protocols
From Benchtop Prototyping to High-Speed Commercial Bottling
Two Purpose-Built Paths to Commercial Scale

Select Your Manufacturing & Go-to-Market Model

Whether you need fast market entry with zero formulation risk or a proprietary clinical compound with exclusive IP ownership, Konnor Health provides tailored engineering roadmaps.

FASTEST TIME-TO-MARKET

Track A: Stock Private Label (White Label)

Designed for fast-growing DTC brands, Amazon e-commerce sellers, and retail chains wanting high-margin, clinically validated nutritional products ready for immediate custom labeling.

300+ Pre-Formulated Master Stock RecipesProven stability profiles for immunity, sleep, anti-aging, nootropics, and metabolic wellness.
Low Capital Risk & Flexible MOQsPilot runs starting at just 500 – 1,000 units to test new market niches without capital stagnation.
2 to 3 Weeks Rapid TurnaroundImmediate production allocation with pre-screened raw materials in current cGMP warehouse inventory.
Complimentary Packaging Dieline & Label AssistancePre-formatted FDA Supplement Facts templates with ingredient %DV declarations ready for your branding.
100% PROPRIETARY IP

Track B: Bespoke Custom Formulation OEM / ODM

Tailored for established nutraceutical enterprises, specialty health brand subsidiaries, and medical practitioners requiring unique active ratios, patented raw materials, and exclusive IP ownership.

100% Custom Formula & IP ProtectionExecute bilateral NDAs first. You retain absolute ownership over your proprietary master batch records.
Active Ingredient Compatibility & Masking TechOvercome astringency, bitter herbal botanical extracts, and microencapsulation of sensitive actives.
Benchtop Lab Sampling in 7–10 DaysPhysical pilot prototypes delivered to your desk for organoleptic taste, aroma, chew, and dissolution approval.
Custom CNC Tooling & Bottle Mold DevelopmentBespoke 3D gummy imprint shapes, custom tablet debossing, and distinctive container industrial molds.
Market-Validated White Label Formulas

High-Demand Private Label Turnkey Formulations

Pre-cleared for microbial, heavy metal, and shelf stability. Ready to bottle with your private label in as little as 14 business days.

Request Full 300+ SKU Formulation Index
TOP SELLER2-3 Weeks Turnaround

Sleep & Stress Restoration

Pectin Gummies / Two-Piece Capsules
Active Profile

Melatonin (3mg/5mg), L-Theanine, Chamomile, GABA, Lemon Balm

From 1,000 UnitsRequest Sample Kit →
HIGH MARGIN2-3 Weeks Turnaround

Metabolic Detox & Digestion

Liquid Dropper / Effervescent / Gummies
Active Profile

Raw Unfiltered ACV (500mg), Mother Culture, Chromium Picolinate, Ginger

From 1,000 UnitsRequest Sample Kit →
TRENDING2-3 Weeks Turnaround

Nootropic Cognitive Focus

Vegetable HPMC Capsules / Powder Sticks
Active Profile

Organic Lion's Mane 10:1, Bacopa Monnieri, Alpha-GPC, Active B-Complex

From 1,000 UnitsRequest Sample Kit →
SEASONAL HERO2-3 Weeks Turnaround

Immune Defense & Shield

Chewable Tablets / Pectin Chews
Active Profile

Elderberry Sambucus Nigra (1000mg equiv), Zinc Citrate, Vitamin C, Echinacea

From 1,000 UnitsRequest Sample Kit →
BEAUTY CORE2-3 Weeks Turnaround

Collagen & Anti-Aging Radiance

Hydrolyzed Powder / Gummies / Liquids
Active Profile

Type I & III Marine Collagen Peptides, L-Glutathione, Hyaluronic Acid, Biotin

From 1,000 UnitsRequest Sample Kit →
CLINICALLY PROVEN2-3 Weeks Turnaround

Active Joint & Mobility Support

Softgels / Enteric Coated Tablets
Active Profile

Glucosamine Sulfate, Chondroitin, Type II Collagen, Turmeric 95% Curcuminoids

From 1,000 UnitsRequest Sample Kit →
Proprietary Engineering & Formulation Science

Contract R&D Lab Capabilities for Custom OEM

From solving difficult active ingredient degradation to eliminating astringent botanical bitterness, our expert nutraceutical formulation scientists engineer shelf-stable, high-bioavailability compounds.

Active Load Optimization

Maximize active loading per unit volume without compromising gummy chew texture, capsule dissolution time, or tablet tensile integrity.

Flavor & Odor Masking

Proprietary organoleptic masking technology eliminates metallic mineral aftertastes and sulfurous botanical odors using plant-derived aroma modulators.

Stability Stress Testing

Accelerated thermal chambers (40°C / 75% RH) and water activity (Aw < 0.65) monitoring to guarantee 24 to 36 months of real-world shelf stability.

7-10 Day Benchtop Sampling

Rapid lab-scale batch compounding allowing your executive team to touch, taste, and evaluate actual physical prototypes before commercial tooling.

Transparent Execution Roadmap

The 6-Step Turnkey Partnership Journey

From non-disclosure agreement to door-to-door global export clearance, every phase is governed by clear cGMP milestones and documented quality sign-offs.

STEP 01

Scoping & Bilateral NDA

We define your formulation goals, target health claims, dosage formats, and packaging requirements under a legally binding bilateral Non-Disclosure Agreement.

STEP 02

Benchtop Lab Prototyping

Our formulation scientists produce physical benchtop prototypes in 7–10 days. Samples are dispatched directly to your team for organoleptic and texture sign-off.

STEP 03

Pilot Run & Stability Assays

Scaling up to an initial pilot run to validate flowability, blend homogeneity, moisture limits, and thermal stress performance under cGMP pilot equipment.

STEP 04

Artwork Dielines & FDA Review

We supply exact engineering dielines and perform in-house regulatory review of your Supplement Facts panels, allergen statements, and legal disclaimers.

STEP 05

cGMP High-Speed Production

Full commercial-scale blending, encapsulation/molding, automated counting, induction sealing, and tamper-evident labeling under Class 100,000 cleanrooms.

STEP 06

Release COA & Global Logistics

Every batch is released with full Certificate of Analysis (COA), 3rd-party heavy metal and microbiological clearance, with DDP/FOB ocean & air export support.

Export Risk Mitigation

Comprehensive Regulatory Advisory & FDA 21 CFR Label Compliance

Importing dietary supplements into North America, Europe, or Southeast Asia requires stringent adherence to national pharmacopeias and packaging disclosure laws. Our regulatory affairs team safeguards your brand before you print.

FDA 21 CFR 101.36 Supplement Facts AlignmentAccurate rounding rules, % Daily Value calculations, proprietary blend disclosures, and linear panel formatting.
FTC-Compliant Structure / Function ClaimsReviewing product marketing claims to ensure permissible wellness statements that prevent FDA warning letters.
FALCPA Allergen Disclosures & Inactive ExcipientsFull transparency for gelatin, soy, gluten, dairy, and artificial coloring cross-contact protocols.
Export Clearance DocumentationBatch COA, Free Sale Certificates (FSC), BSE/TSE statements, Non-GMO certificates, and Halal/Kosher documentation.

cGMP Analytical Verification Standard

Every production release complies with 4-point lab testing

1. Heavy Metals (ICP-MS)Lead, Arsenic, Cadmium, Mercury < USP Limits
2. Microbial Screen (USP <2021>)Negative E. coli, Salmonella, S. aureus
3. Active Potency (HPLC / UV-Vis)100% - 120% Target Claim Assurance
4. Physical DisintegrationCompliant with USP <2040> Pharmacopeia
Need a sample Certificate of Analysis?Download Sample COA Package →
Clarifying Procurement Doubts

Frequently Asked Procurement & Formulation Questions

Everything you need to know about MOQs, formula ownership, lead times, and confidentiality.

Direct Formulation Consultation

Start Your Private Label or Custom OEM Project

Submit your project parameters below. Our technical formulation managers will review your active ingredient targets and deliver a structured quotation and sampling plan within 12 business hours.

Bilateral Non-Disclosure Agreement (NDA) executed on request
Benchtop prototypes dispatched in 7–10 days
Zero formulation spam. Direct technical engineering response.
Instant WhatsApp Technical Hotline
+86 15992025243 (Direct with Lead Project Chemist)

By submitting, you agree to our confidential formulation handling under mutual non-disclosure principles.