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GALEGA OFFICINALIS EXTRACT.

Insufficient Data CAS 84650-07-7 / SKIN CONDITIONING

Galega Officinalis Extract, derived from Goat's Rue, is a multi-functional botanical ingredient recognized for its anti-aging, antioxidant, and skin-conditioning properties. It leverages phytoestrogens and beta-sitosterol to support skin health and resilience.

antioxidant skin-conditioning anti-aging anti-inflammatory regenerating immunomodulatory antiseptic

Science

This extract functions by engaging with skin's estrogen receptors via its phytoestrogen content, stimulating collagen production and enhancing dermal elasticity to counteract premature aging. Its rich beta-sitosterol profile provides immunomodulatory, antiseptic, anti-inflammatory, regenerating, and antioxidant benefits. In vitro studies further indicate that its flavonols and hydroxycinnamic acids possess potent antiradical activity, while guanidines and flavonoids effectively trap methylglyoxal (MGO), contributing to overall antioxidative defense.


Research

Low confidence
Effective range N/A
Optimal

N/A


Transparency

Not commonly dusted

The Formula

Solubility
Water
Optimal pH N/A
0 7 14

Stability

Aqueous extracts are naturally free from essential oils and declarable fragrance allergens. Formulations containing its polyphenolic components may exhibit enhanced stability within a slightly acidic pH range.


Safety

CIR Status
Not reviewed
Sensitization risk Unknown

Comprehensive safety data, including GHS classification for hazards, dermal toxicity, oral toxicity, and inhalation toxicity, has not been determined. It has not been formally assessed by the Cosmetic Ingredient Review (CIR), SCCS, or listed as Generally Recognized As Safe (GRAS) by the FDA for cosmetic applications.


Your Skin

Yes Normal
Yes Dry
Yes Oily
Yes Sensitive
Irritancy Unknown
Comedogenicity Unknown

Our Assessment

Insufficient Data

Galega Officinalis Extract presents promising multi-functional benefits in vitro, particularly for anti-aging and antioxidant defense, however, a lack of human clinical studies and comprehensive safety assessments by regulatory bodies necessitates further research for full endorsement.


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