Certificates

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Skin Sensitization Evaluation – ISO 10993-10

Assessed using the closed-patch (Buehler) test method under ISO 10993-10 standards. No skin sensitization reactions were observed during controlled testing.

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Dermal Irritation Assessment – ISO 10993-23

Tested according to internationally recognized ISO 10993-23 irritation standards. Under laboratory conditions, the product demonstrated negligible irritation response, supporting its suitability for topical application.

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Preservative System Effectiveness Verified (USP <51>)

Tested according to United States Pharmacopeia (USP-NF Chapter 51) antimicrobial effectiveness standards. The formulation demonstrated effective protection against bacteria, yeast, and mold to ensure product stability and safety over time.

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Heavy Metal Safety – Regulatory Compliance Verified

Tested for Lead (Pb) and Mercury (Hg) in accordance with California Proposition 65, Washington Toxic-Free Cosmetics Act (2025), and US FDA 21 CFR 700.13 requirements. Results confirmed compliance within regulated safety limits.

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Microbiologically Tested & Within Safety Limits

Evaluated under USP <61> & <62> microbiological standards and PCPC cosmetic guidelines. The product met limits for total aerobic count, yeast and mold, and showed absence of specified pathogenic microorganisms.

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Clinically Tested for Long-Lasting Performance

Independently evaluated in a 60-day supervised human use study. The product demonstrated strong consumer satisfaction, effective odor control performance, and no reported adverse events under test conditions. Conducted by a certified third-party laboratory.

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In Vitro Biocompatibility Assessment

Evaluated using standardized cell culture testing methods to assess cytotoxic response. Results indicated no significant cytotoxic effects under controlled laboratory conditions.

Skin Sensitization Evaluation – ISO 10993-10

Assessed using the closed-patch (Buehler) test method under ISO 10993-10 standards. No skin sensitization reactions were observed during controlled testing.

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Dermal Irritation Assessment – ISO 10993-23

Tested according to internationally recognized ISO 10993-23 irritation standards. Under laboratory conditions, the product demonstrated negligible irritation response, supporting its suitability for topical application.

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Preservative System Effectiveness Verified (USP <51>)

Tested according to United States Pharmacopeia (USP-NF Chapter 51) antimicrobial effectiveness standards. The formulation demonstrated effective protection against bacteria, yeast, and mold to ensure product stability and safety over time.

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Heavy Metal Safety – Regulatory Compliance Verified

Tested for Lead (Pb) and Mercury (Hg) in accordance with California Proposition 65, Washington Toxic-Free Cosmetics Act (2025), and US FDA 21 CFR 700.13 requirements. Results confirmed compliance within regulated safety limits.

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Microbiologically Tested & Within Safety Limits

Evaluated under USP <61> & <62> microbiological standards and PCPC cosmetic guidelines. The product met limits for total aerobic count, yeast and mold, and showed absence of specified pathogenic microorganisms.

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Clinically Tested for Long-Lasting Performance

Independently evaluated in a 60-day supervised human use study. The product demonstrated strong consumer satisfaction, effective odor control performance, and no reported adverse events under test conditions. Conducted by a certified third-party laboratory.

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In Vitro Biocompatibility Assessment

Evaluated using standardized cell culture testing methods to assess cytotoxic response. Results indicated no significant cytotoxic effects under controlled laboratory conditions.