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Moumoujus

HYDROLYZED LIMONIUM LATIFOLIUM.

Insufficient Data CAS - / SKIN PROTECTING

Derived from sea lavender, Hydrolyzed Limonium Latifolium is a multi-functional ingredient known for its robust antioxidant and anti-inflammatory properties. It actively hydrates the skin, supports collagen synthesis, and helps to minimize the appearance of fine lines, promoting a more even and radiant complexion.

Summary

antioxidant moisturizing anti-inflammatory skin-conditioning

Science

Mechanism of Action

This ingredient operates by delivering a rich profile of antioxidants and polyphenols to the skin, effectively neutralizing free radicals and protecting against oxidative stress. It exhibits significant anti-inflammatory actions, which diminish visible redness and irritation. Furthermore, it enhances skin's moisture retention by attracting water molecules and reinforcing the skin's natural barrier, leading to improved elasticity. Its capacity to stimulate collagen synthesis also contributes to visible reduction in fine lines and a refined skin texture.

Research

Clinical Evidence

Low confidence
Effective range N/A
Optimal

N/A

Transparency

Dusting Analysis

Not commonly dusted

The Formula

Formulation

Solubility
Unknown
Optimal pH N/A
0 7 14

Safety

Safety Profile

CIR Status
Not reviewed
Sensitization risk Low

The Cosmetic Ingredient Review (CIR), Scientific Committee on Consumer Safety (SCCS), and FDA have not conducted specific safety assessments or issued status reports for Hydrolyzed Limonium Latifolium. While general 'sea lavender' is often described as allergen-free and suitable for all skin types, this assessment does not officially extend to the hydrolyzed form, indicating a lack of specific regulatory review for this ingredient variant.

Your Skin

Skin Compatibility

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

Our Assessment

Verdict

Insufficient Data

While demonstrating significant potential benefits including antioxidant, anti-inflammatory, and moisturizing effects, comprehensive clinical data and regulatory safety assessments for the hydrolyzed form are currently insufficient for a definitive rating.

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