Source Valerian Root Extract for Your Supplement Brand

Specifications

Target specifications may include standardized valerenic-acid assays or extract ratios. Botanical identity, plant part, assay, extraction solvent, carrier, and destination-market compliance are confirmed in the RFQ and supplier COA.

Certifications

Facility licensing, certifications, and available quality or export documents are confirmed for each matched manufacturer and product classification.

MOQ

Confirmed after formula, format, packaging, volume, and target-market review.

Formats

Potential formats include capsules, tablets, gummies, liquid shots, and powder sticks. Feasibility depends on dose, taste, stability, solubility, and destination-market requirements.

Lead Time

Sampling and production timelines are confirmed after specification, formulation, and packaging review.

Regulatory Note

Regulatory classification and permitted claims depend on the exact ingredient specification, product category, and destination market.

Clinical Research

metaAmerican Journal of Medicine · 2006

Valerian for Sleep: A Systematic Review and Meta-AnalysisSuggests possible subjective sleep-quality improvement; the authors report methodological problems in most studies and evidence of publication bias.

rctJournal of Supportive Oncology · 2011

The use of Valeriana officinalis (valerian) in improving sleep in patients who are undergoing treatment for cancer: a phase III randomized, placebo-controlled, double-blind study (NCCTG Trial, N01C5)Phase III trial in cancer patients; no significant improvement in the primary PSQI sleep-quality endpoint, with improvement only in some exploratory secondary measures such as fatigue.

Each paper links to its original PubMed record.

Buyer FAQ

Q. What should I include in a quote request?

Target specification (extract ratio or valerenic-acid assay), dosage format, dose per serving, estimated volume, packaging, and destination market. Complete RFQs match faster and quote more accurately.

Q. What quality documents are available?

Document availability (COA, facility licensing, certifications, export documents) is confirmed for each matched manufacturer and product classification.

Q. How do you confirm whether a valerian product is eligible in South Korea and what claims it can use?

We do not classify a valerian project from the common name alone. Eligibility and permitted claims depend on the exact botanical, plant part, extract specification, product category, and destination market. These requirements are confirmed during formulation review.

Q. Why aren't MOQ and lead time listed upfront?

Both depend on formula, format, packaging, volume, and target market. They are confirmed after feasibility review with the matched manufacturer, so quoted numbers reflect your actual project rather than a generic range.

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