Valerian root 500 mg — herbal powder hard capsules · CGR-ES-119 (CGR-ES-119)

REFERENCE FORMULA

Reference formula

Reference basis: 1 capsule as reference unit; for N capsules: 500 × N mg herbal powder

Ingredient	Source quantity	Scaled quantity
Valerian root powder	500 mg / capsule	—
Empty hard capsule; source suggests size 00	1 unit / capsule	—

Prerequisite formulations

No separate prerequisite monograph is listed.

Documentation

Preparation description

Each unit contains 500 mg of identified herbal powder, without extraction or added solvent. Herbal-drug mass is not equivalent to extract mass or isolated constituent mass. Record capsule-shell composition separately. ^{[1], [2], [3]}

Action and use

For powdered root, HMPC recognises traditional relief of mild mental-stress symptoms and assistance with sleep. Well-established use concerns a specific ethanolic dry extract, not these capsules. HMPC powder intake is 0.3–2.0 g; the older Spanish instruction of up to six 500-mg capsules (=3 g) is not adopted. Confirm the final regimen for powdered material. ^{[1], [3]}

Specifications

Accept raw material against RFE/Ph.Eur. monograph 0453 with species, plant-part and lot verification. Finished-unit controls include secure closure, absence of exterior powder, mass uniformity and disintegration requirements. Obtain numerical acceptance criteria from the current pharmacopoeia. ^{[2], [4], [5]}

Light

Protect raw material and capsules from light through opaque secondary packaging or a suitable light-protective container. A quantitative photostability study of this exact formulation/lot was not identified. ^{[1], [2], [5]}

Air and oxidation

The drug contains volatile constituents and has a strong odour. Closed containers and brief handling limit volatile loss and odour transfer to other preparations. No numerical oxygen or inert-atmosphere specification was established. ^{[2], [5]}

Water and solubility

Add no water during filling. Wet equipment can promote clumping and impair the shell; document complete drying after cleaning. Water used for swallowing does not convert this capsule into a stored aqueous preparation. ^{[4], [5]}

Humidity

Preparation environment: relative humidity not above 60% and temperature 25±5 °C, subject to stricter drug/shell requirements. Protect the packed product from moisture. Room relative humidity is not a product water-activity measurement. ^{[1], [4]}

Temperature

Source storage is below 30 °C. Avoid extra heating, direct sunlight and prolonged hot milling. Refrigeration is not specified; opening a cold container may introduce condensation and requires separate assessment. ^{[1], [2], [5]}

pH and compatibility

No pH is specified for the dry capsule. A suspension pH, if selected as a test, requires a defined powder-to-water ratio and method; it is not automatic evidence of stability or clinical activity. ^{[1], [5]}

Other interactions

AEMPS cautions about alcohol and other CNS depressants; HMPC states no reported interactions. Co-treatment and sedation still require assessment. This powder formula contains no ethanol or extraction solvent. ^{[1], [3]}

Ingredient-specific information

The drug comprises dried underground organs of Valeriana officinalis: rhizome, roots and stolons. AEMPS specifies at least 0.17% sesquiterpenic acids expressed as valerenic acid on dry-drug basis. Obtain current essential-oil/marker tests from the pharmacopoeia. Characteristic strong odour alone does not establish purity or potency. ^{[2], [3], [5]}

Staff protection

Use a controlled work area, limit airborne powder, wear gloves and protective clothing, and eye protection where powder splashing is foreseeable. The dust assessment determines extraction and suitable respiratory protection. Do not clean using compressed air or dry sweeping. ^{[4], [5]}

Risk assessment

Hypersensitivity is contraindicated. Not recommended under 12 or in pregnancy/lactation. It may impair driving/machinery operation and cause nausea or abdominal cramps. Assess sedation with other treatments and alcohol. Laboratory risks include extract-for-powder substitution, excessive unit/regimen, repeated exposure to odorous dust and cross-contamination. ^{[1], [3], [5]}

Compounding conditions

Verify cleanliness, full dryness, material identity/expiry and an approved calculation. For N units, theoretical herbal-powder mass=500×N/1000 g. Record actual sieving losses; do not apply arbitrary active overfill. ^{[1], [4]}

BUD rationale

The source gives 3 months under its storage conditions. The register uses a conservative ceiling of 89 days, not exceeding 3 calendar months or the earliest ingredient expiry, below 30 °C and protected from light/moisture. This is an official formula validity period, not experimentally demonstrated stability of locally produced capsules. No study matching herbal drug, particle size, shell and container was found. Selection does not assume aw<0.60 or automatically apply the 180-day general ceiling. Extension or different packaging requires evidence for marker/fingerprint, disintegration, moisture and microbiological quality. Editorial convention: calendar-month source periods are retained as calendar periods; the calendar-period conversion ceiling is 28 days for one month or 89 days for three months; a separately selected shorter ceiling still governs. It is a conservative conversion, not a source quotation. ^{[1], [5], [6]}

Prerequisites

Use locally approved weighing, sieving, capsule-filling, cleaning, testing and labelling SOPs. This formula mandates no prepared excipient from the existing register. Adding diluent creates a separately documented variant with explicit quantity and controls. ^{[1], [4]}

Equipment

Calibrated balance suitable for batch size, 355-µm sieve, fully dry mortar/mixer, graduated cylinder for apparent bulk volume, spatula and capsule-filling device. Actual apparent density and capsule-shell specifications determine capacity. ^{[1], [4]}

Compounding method

1. Verify dry-drug identity and batch mass. 2. Break agglomerates, sieve through 355 µm and record recovery. 3. Measure apparent bulk volume and verify that the target charge fits source-suggested size 00. 4. Homogenise, fill to provide 500 mg drug per unit, and close. 5. Remove exterior powder, test and package. If another size or excipient is needed, document the change before execution. ^{[1], [4]}

Observations

The active material is whole herbal powder of the specified plant part. Do not substitute dry extract, essential oil or unspecified “equivalent” botanical material. Gross capsule mass includes the shell; assess net fill separately in uniformity work. ^{[1], [2], [3], [4]}

Container and packaging

The official formula permits blister packaging or a tightly closed bottle. Select a pharmaceutical container with documented moisture barrier and light protection; no particular polymer is mandated by the source. Use a desiccant only when shell-compatible, separated from capsules and appropriately labelled. ^{[1], [4], [5]}

Quality control

Verify drug authenticity and CoA through appropriate identity/marker confirmation. Finished-product controls: appearance, closure, unit count, net fill and mass uniformity under current RFE 2.9.5. For batches, the source procedure additionally specifies disintegration and microbiological testing. Shelf-life adoption also considers fingerprint/marker and moisture change. These tests have not been performed in this literature work. ^{[2], [4], [5]}

Storage

Below 30 °C, protected from light and moisture, with immediate reclosure after each use. Reject or investigate sticking units, soft/cracked shells or visible moisture; judge the botanical-specific odour against an approved reference. ^{[1], [2], [4]}

Dispensing

Confirm powdered-drug dose and concomitant sedatives. Warn against driving or operating machinery when affected. No definitive timing is taken from a different extract study. Persistent/worsening insomnia or mental-stress symptoms require clinical assessment; the Spanish source advises review beyond 2 weeks. ^{[1], [3]}

Labelling

Valerian root 500 mg/capsule. Oral use. Dose and duration: follow the responsible professional’s individual directions. Batch:____. Prepared:____. Use by:____. Below 30 °C; protect from light/moisture. Keep out of children’s reach. Declare full shell composition and any added excipients. May cause drowsiness; do not drive/operate machinery if affected. ^{[1], [3], [4]}

v9_controls

The numeric value is a literature reference ceiling subject to its specific conditions. No actual batch BUD has been assigned and no aw measurements have been produced. The exact formula, prerequisites, container, storage and quality evidence require approval for the actual application. The BUD clock starts when compounding begins. Use the shortest applicable supported limit and assess in-use dating separately. USP categories are a technical framework and are not presented as Greek legislation.

Independent Greek/English scientific synthesis crediting AEMPS with supporting evidence. This is not an official translation, marketing authorisation or publisher endorsement. Stasinos Chr.Sikalias — compounding.gr.

Sources and references

AEMPS Formulario Nacional — FN/2003/POF/014 RAÍZ DE VALERIANA, CÁPSULAS DURAS DESource code FN/2003; current standalone official PDF retrieved 13 October 2026PDF pp.2–4; sections 3–12Exact master formula, process, storage, source validity period; older clinical details reassessed using reference 32026-10-14
AEMPS Formulario Nacional — FN/2003/PAF/014 VALERIANA, RAÍZ DESource code FN/2003; official standalone PDF retrieved 13 October 2026PDF p.2; identity, composition, raw-material specification and handlingBotanical raw-material identity and source-era specifications; current pharmacopoeial specification must be consulted before acceptance2026-10-14
EMA/HMPC — European Union/Community herbal monograph on Valeriana officinalis L., radix2 February 2016; EMA/HMPC/150848/2015, Corr.1PDF pp.3–9; preparation categories, sections 4.1–4.8Current adopted regulator monograph for specific plant part and preparation; not approval of this compounded product or product-specific stability evidence2026-10-13
AEMPS — PN/L/FF/001/00 Elaboración de cápsulas durasPN/L/FF/001/00; official standalone PDF retrieved 13 October 2026PDF pp.4–5; sections 4.3–4.6Capsule preparation, measured bulk-volume approach, environment, mass uniformity, disintegration and microbiological controls2026-10-13
EMA — Guideline on quality of herbal medicinal products/traditional herbal medicinal products, revision 318 January 2022; EMA/HMPC/CHMP/CVMP/201116/2005 Rev.3PDF pp.9–10 and 12–16; sections 5.1,7,8Identity, contaminants, justified specifications, chromatographic fingerprint and multi-component stability principles; numerical shelf life not supplied2026-10-13
USP Compounding Expert Committee — USP Compounding Webinar, NABP public handout14 September 2023; primary-author public educational handoutPDF pp.10–11, slides 19–22General aw-dependent BUD framework comparator; not full licensed USP795 text, Greek law, or measured stability/aw for this formulation2026-10-13
USP — General Chapter <795> Frequently Asked QuestionsNovember 1, 2023 FAQ; rechecked 14 October 2026Questions 52, 54–56, 61, 64–66General category/extension rules only; not exact-product stability evidence.2026-10-14