Botanical Capsules
HPMC vegetable, pullulan, and gelatin capsules in sizes 000 through 4. Options for delayed-release, liquid-filled, or banded capsules to protect sensitive herbal extracts.
Bactolac Pharmaceutical, Inc. is a premier contract manufacturer specializing in custom private label herbal supplements and standardized botanical extracts. For over three decades, global brand owners, healthcare chains, and cross-border importers have partnered with our New York facility to build market-leading dietary supplement lines.
Because herbal ingredients present unique challenges in flowability, identity, moisture sensitivity, and potency preservation, our in-house formulation scientists and analytical chemists rigorously test every raw material lot. We ensure your finished botanical formulations strictly comply with FDA cGMP, NSF, and global regulatory standards.
Consumer demand for clean, natural, and standardized herbal supplements is growing rapidly across North America, Europe, Asia, and the Middle East. However, raw botanical sourcing requires specialized expertise to prevent adulteration, species substitution, or micro-contamination.
At Bactolac Pharmaceutical, our quality control system protects your brand reputation by enforcing end-to-end traceability and strict regulatory compliance from farm to finished package.
Our 200,000+ square foot automated facility is engineered to process complex botanical formulas into high-demand finished dosage formats with tight precision.
HPMC vegetable, pullulan, and gelatin capsules in sizes 000 through 4. Options for delayed-release, liquid-filled, or banded capsules to protect sensitive herbal extracts.
Chewable, sublingual, time-release, bi-layer, and color-coated tablets engineered for optimal disintegration rate, minimal friability, and active compound release.
High-shear ribbon blending for superfood greens, red berry antioxidant mixes, adaptogenic mushroom powders, and instantized herbal tea blends.
Botanical seed oils, liposomal herbal complexes, and fat-soluble herbal formulations delivered in hermetically sealed softgel capsules.
USDA Organic, Non-GMO Project Verified, allergen-free, vegan, Kosher, and Halal production under segregated cGMP protocols.
Wide-mouth HDPE/PET bottles, glass jars, gusset bags, blister packs, and single-serve stick packs with tamper-evident induction sealing.
Our R&D scientists routinely formulate, benchmark, and scale production for leading wellness categories targeted by international buyers.
Ashwagandha, Rhodiola Rosea, Holy Basil, and Ginseng formulations optimized for cortisol control and energy balance.
Elderberry, Echinacea, Astragalus, and Medicinal Mushroom complexes (Reishi, Lion's Mane, Cordyceps) with standardized beta-glucans.
Bacopa Monnieri, Ginkgo Biloba, Gotu Kola, and green tea extracts standardized for EGCG and L-Theanine.
Berberine HCl, Cinnamon extract, Gymnema Sylvestre, and Bitter Melon engineered for healthy glucose and weight management.
Deglycyrrhizinated Licorice (DGL), Ginger root, Peppermint, Aloe Vera, and herbal liver detox matrices (Milk Thistle, Artichoke).
Black Cohosh, Chasteberry, Saw Palmetto, Fenugreek, and Maca root tailored for hormonal balance and vitality.
Turmeric Curcumin (95% curcuminoids), Boswellia Serrata, Ginger, and Tart Cherry extracts with enhanced bio-availability.
Valerian Root, Passionflower, Chamomile, Lemon Balm, and Magnolia Bark engineered for rapid sleep onset.
Botanical contract manufacturing requires continuous analytical oversight to prevent batch-to-batch variation and safety non-compliance. Bactolac operates two state-of-the-art analytical and microbiological laboratories within our Hauppauge, New York facility.
Every single batch of private label herbal supplements is thoroughly verified before release, guaranteeing that finished products match label claims and conform strictly to global import regulations.
Our manufacturing practices adhere strictly to US FDA 21 CFR Part 111 guidelines. We maintain comprehensive voluntary certifications to streamline regulatory approval for international markets.







Importing dietary supplements requires precise regulatory documentation to ensure seamless clearance through customs in Europe, Asia, the Middle East, and the Americas. Bactolac’s dedicated export documentation team simplifies cross-border sourcing.
Our streamlined contract manufacturing workflow provides complete transparency and strict milestones at every step of your project.
Review target formula, botanical standardized markers, target dosage form, MOQs, budget, and target market regulations.
R&D scientists optimize blend flowability, excipient compatibility, and organoleptic parameters; sample issued.
Botanicals are quarantined, identity-tested, and screened for heavy metals, pesticides, and microbial limits in our lab.
Precision weighing, high-shear blending, encapsulation or tableting, coating, bottling, and tamper-evident sealing.
Final analytical assay, COA issuance, CFS generation, export palletization, and shipping release for your freight forwarder.
Answers to common questions regarding private label herbal supplement contract manufacturing, compliance, and minimum order quantities.
Dietary supplements do not require pre-market approval from the US FDA. However, the manufacturer must strictly comply with FDA 21 CFR Part 111 cGMP regulations governing facility cleanliness, raw material identity testing, master manufacturing records, and finished product specification release. Bactolac provides complete audit reports and documentation packages confirming strict cGMP adherence.
We perform 100% raw material quarantine and identity testing on all incoming herbal powders and extracts. Utilizing High-Performance Liquid Chromatography (HPLC), Thin-Layer Chromatography (TLC), and FTIR spectroscopy in our on-site laboratories, we authenticate species identity, measure active phytochemical levels, and screen out adulterants or synthetic substitutes.
Our standard export documentation package includes a lot-specific Certificate of Analysis (COA), Certificate of Free Sale (CFS), cGMP Compliance Certificate, Allergen Statement, Non-GMO Declaration, BSE/TSE Free Statement, and Manufacturing Flowchart required by foreign health authorities.
Standard production MOQs start around 25,000 units for capsules and tablets, and 1,000 kg for powder blends. Pilot launch runs can be reviewed on a case-by-case basis. Standard turnaround time is 6 to 10 weeks following final specification sheet approval and packaging receipt, depending on raw material sourcing leads.
Yes. Our R&D chemists specialize in formulating clean-label herbal supplements without magnesium stearate, artificial colors, or synthetic preservatives. We offer certified organic manufacturing under USDA organic protocols, utilizing rice flour or organic acacia gum as natural flow agents.
Connect with our technical team to request product specifications, custom pricing, or request a complete product catalog.