Garlic - ALLIUM SATIVUM

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This monograph is intended to serve as a guide to industry for the preparation of Product Licence Applications (PLAs) and labels for natural health product market authorization. It is not intended to be a comprehensive review of the medicinal ingredient.

Notes

Date

March 31, 2023

Proper name(s), Common name(s), Source information

Garlic dried bulb
Table 1. Proper name(s), Common name(s), Source information
Proper name(s) Common name(s) Source information
Source material(s) Part(s) Preparation(s)
Allium sativum Garlic Allium sativum Bulb Dry

References: Proper name: USDA 2018; Common name: McGuffin et al. 2000; Source information: ESCOP 2003, Bradley 1992.

Garlic essential oil

Table 2. Proper name(s), Common name(s), Source information
Proper name(s) Common name(s) Source information
Source material(s) Part(s)
Allium sativum Garlic essential oil Allium sativum Bulb

References: Proper name: USDA 2018; Source information: ESCOP 2003, Bradley 1992.

Route of administration

Oral

Dosage form(s)

This monograph excludes foods or food-like dosage forms as indicated in the Compendium of Monographs Guidance Document.

Acceptable dosage forms by age group:

Children 2 years: The acceptable dosage forms are limited to emulsion/suspension and solution/ liquid preparations (Giacoia et al. 2008; EMEA/CHMP 2006).

Children 3-5 years: The acceptable dosage forms are limited to chewables, emulsion/ suspension, powders and solution/liquid preparations (Giacoia et al. 2008; EMEA/CHMP 2006).

Children 6-11 years, Adolescents 12-17 years, and Adults 18 years and older: The acceptable dosage forms for oral use are indicated in the dosage form drop-down list of the web-based Product Licence Application form for Compendial applications.

Use(s) or Purpose(s)

The following combined use(s) or purpose(s) is/are also acceptable:

Notes
Claims for traditional use must include the term "Herbal Medicine", "Traditional Chinese Medicine", or "Ayurveda".

Dose(s)

Subpopulation(s)

As specified below

Quantity(ies)

Methods of preparation: Dry, Powdered, Non-Standardized Extracts (Dry extract, Tincture, Fluid extract, Decoction, Infusion)

Table 3. Dose information for garlic bulb presented as dose per day
Subpopulation(s)1,2 Garlic bulb (g/day)
Minimum Maximum
Children
2-4 years 0.08 2
5-9 years 0.1 3
10-11 years 0.2 6
Adolescents
12-14 years 0.2 6
15-17 years 0.5 12
Adults 18 years and above 0.512

1 Children and adolescent doses were calculated as a proportion of the adult dose (JC 2008). The use of garlic in children is supported by the following references: McIntyre 2005; Bove 2001; Schilcher 1997.
2 Adult dose supported by the following references: Kojuri et al. 2007; Mills and Bone 2005; ESCOP 2003; Kannar et al. 2001; Blumenthal et al. 2000; Bradley 1992.

Methods of preparation: Standardized extracts (Dry extract, Tincture, Fluid extract, Decoction, Infusion)

Table 4. Dose information for allicin and alliin presented as dose per day. Extracts should be standardized to allicin and/or alliin.
Subpopulation(s)1,2 Minimum (mg/day) Maximum (mg/day)
Allicin Alliin Allicin Alliin
Children
2-4 years 0.17 0.324.5
5-9 years 0.25 0.537
10-11 years 0.5 1614
Adolescents
12-14 years 0.5 1614
15-17 years 1 21227
Adults18 years and above 1 21227

1 Children and adolescent doses were calculated as a proportion of the adult dose (JC 2008). The use of garlic in children is supported by the following references: McIntyre 2005; Bove 2001; Schilcher 1997.
2Adult dose for allicin supported by the following references: Kojuri et al. 2007; Mills and Bone 2005; ESCOP 2003; Kannar et al. 2001; Bradley 1992. Adult dose for alliin calculated based on the conversion ratio of 0.45 mg allicin: 1 mg alliin (ESCOP 2003).

Method of preparation: Oil, Essential (water steam distillation)

Table 5. Dose information for garlic essential oil presented as dose per day
Subpopulation(s) Garlic essential oil (mg/day)
Minimum Maximum
Adults1 18 years and above 2 5

1Adult dose supported by the following reference: Bradley 1992.

Direction(s) of use

No statement required

Combination rule

No permitted combinations between ingredients from Table 1 and 2. This monograph only supports single ingredient products for compendial applications.

Duration (s) of use

No statement required.

Risk information

Caution(s) and warning(s)

Relief of upper respiratory tract infections and catarrhal (nasal congestion) conditions

Consult a health care practitioner if symptoms persist or worsen.

All uses

Contraindication(s)

No statement required.

Known adverse reaction(s)

Stop use if hypersensitivity/allergy occurs (Brinker 2018; Mills and Bone 2005).

Non-medicinal ingredients

Must be chosen from the current Natural Health Products Ingredients Database (NHPID) and must meet the limitations outlined in the database.

Storage conditions

Must be established in accordance with the requirements described in the Natural Health Products Regulations (NHPR).

Specifications

References cited

References reviewed