At her®, we believe that what you put into your body should be held to an absolute, uncompromised standard. That's why we operate a rigorous, multi-phase testing architecture that intentionally goes above and beyond foundational industry rules. We don't design for superficial benchmarks; we engineer for radical precision.
Our structural dedication to safety is anchored in clinical data justification, maximum bioavailability validation, and absolute transparency. From our foundational sourcing down to the final production cycle managed by KMM Marcena Trading, every batch of Glow Essentials® is thoroughly analyzed to give you an undeniable foundation for systemic health, cell longevity, and raw vitality.
Third-Party Certifications
Independent, third-party authentication forms the non-negotiable bedrock of our quality controls. Our alignment with the regulatory parameters of the Philippine Food and Drug Administration (FDA) is anchored by a comprehensive Technical Dossier. This critical blueprint details our scientific safety arguments, ingredient bioavailability profiles, and rigorous processing parameters.
The validation of this Technical Dossier is what legally unlocks our official License to Operate (LTO) and Certificate of Product Registration (CPR). By making these records accessible, we bridge the gap between advanced cosmetic science and empirical regulatory accountability.
Republic of the Philippines
Department of Health
FOOD AND DRUG ADMINISTRATION
Civic Drive, Filinvest Corporate City
Alabang, Muntinlupa City
Food and Drug Administration
PHILIPPINES
LICENSE TO OPERATE
as Food Distributor-Exporter/Importer/Wholesaler
is hereby granted to
KMM MARCENA TRADING
#78-C Sct. De Guia St., Laging Handa 4, Quezon City, Metro Manila
Owner: Khristine Marie Mae Redondo Marcena
License Number: CFRR-NCR-FI/E/W-93364
Application Type: Renewal
Date of Issuance: 19 June 2023
Validity of License: 20 August 2028
This LTO shall be renewed within 90 days before its expiration, upon compliance with relevant laws, rules and regulations and the payment of fees. This LTO may be suspended, cancelled or revoked by this Office for cause if found violating RA 9711 and related issuances.
Furthermore, with this LTO, the FDA allows the establishment to apply for a market authorization [i.e. registration (CPR) or notification] for health products prior to manufacture, importation, sale or offer for sale, distribution, transfer and advertisement as the case may be.
DR. SAMUEL A. ZACATE
Director General
Republic of the Philippines
Department of Health
FOOD AND DRUG ADMINISTRATION
BAGONG PILIPINAS
FDA Registration No.: FR-4000015719362
CERTIFICATE OF PRODUCT REGISTRATION
Brand Name: HER®
Product Name: GLOW ESSENTIALS® S-ACETYL GLUTATHIONE + C-LIPID & CoQ10 COMPLEX
(Registered as Food Supplement with NO APPROVED THERAPEUTIC CLAIMS)
Packaging: 150 ML HDPE WHITE SEALED BOTTLE PACKED IN CARTON BOX
Company Name and Address: KMM MARCENA TRADING, #78-C Sct. De Guia St., Laging Handa 4, Quezon City, Metro Manila
LTO No.: CFRR-NCR-FI/E/W-93364
Issued on 06 March 2026 and valid until 06 March 2028.
BY AUTHORITY OF THE DIRECTOR GENERAL:
PILAR MARILYN M. PAGAYUNAN
Director IV, Center for Food Regulation and Research
Certificate of Analysis & Stability
Potency over time requires empirical proof. To confirm that the premium active molecular concentrations in Glow Essentials® remain entirely stable and highly bioavailable throughout their shelf life, we maintain dual stability tracking tracks.
Our completed Accelerated Stability Testing program (monitored windows: 2025.11.10 – 2027.11.09) applies heightened thermal and environmental stressors to guarantee long-term formula preservation. Parallel to this, we execute a strict Real-Time Stability Testing sequence on our live production batches. This real-time logging records product integrity at fixed 3-month, 6-month, 9-month, and 12-month intervals, transitioning to bi-annual reviews thereafter. Our latest current production milestone was successfully cleared and archived last month.
MATERIAL SAFETY DATA SHEET
HER® GLOW ESSENTIALS® S-ACETYL GLUTATHIONE + C-LIPID & CoQ10 COMPLEX
KMM MARCENA TRADING
LTO No.: CFRR-NCR-FI/E/W-93364
FDA Registration No.: FR-4000015719362
SECTION 1: Identification
Product name: GLOW ESSENTIALS® S-ACETYL GLUTATHIONE + C-LIPID & CoQ10 COMPLEX
Brand: HER®
Company: KMM MARCENA TRADING
SECTION 2: Hazards identification
Not a hazardous substance or mixture according to Regulation (EC) No. 1272/2008.
SECTION 3: Composition/information on ingredients
Active Complex:
- S-Acetyl Glutathione
- Alpha Lipoic Acid
- Coenzyme Q10
- Vitamin E (as Tocotrienols)
- Ascorbyl Palmitate (Fat-Soluble Vitamin C)
Regulatory Note: No components need to be disclosed according to the applicable regulations.
SECTION 4: First aid measures
If inhaled: Move the person into fresh air.
In case of skin contact: Wash off with soap and plenty of water.
In case of eye contact: Flush eyes with water as a precaution.
If swallowed: Never give anything by mouth to an unconscious person. Rinse mouth with water.
SECTION 5 & 6: Firefighting & Accidental release measures
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Environmental precautions: Do not let product enter drains.
SECTION 7: Handling and storage
Conditions for safe storage: Store in a cool place. Keep the container tightly closed in a dry and well-ventilated place.
Recommended storage temperature: Below 30°C
SECTION 9: Physical and chemical properties
Appearance Form: Softgels
Colour: Dark green transparent soft capsules
Melting/Boiling point: No data available
pH: No data available
SECTION 10: Stability and reactivity
Chemical stability: Stable under recommended storage conditions.
Incompatible materials: Strong oxidizing agents.
SECTION 11: Toxicological information
Acute toxicity: LD50 Oral - Mouse - 5,000 mg/kg
Carcinogenicity (IARC): No component of this product present at levels greater than or equal to 0.1% is identified as probable, possible or confirmed human carcinogen by IARC.
Heavy Metals
Elemental safety is crucial for any product intended for long-term, daily oral consumption. Environmental contaminants can slowly accumulate over time, presenting real health risks. To combat this, we screen our formulations using high-sensitivity Inductively Coupled Plasma Mass Spectrometry (ICP-MS) down to parts-per-billion (ppb), confirming limits sit well below standard local and international safety thresholds.
We purposely formulate without cross-reactive ingredients or common allergens. Our advanced processing hubs execute strict, physical line isolation and validated equipment washdowns to avoid particulate migration. We deliberately run these verification steps to ensure our bioavailable anti-aging nutrients remain clean, safe, and highly accessible for sensitive individuals.
CROSS-CONTAMINATION SCREENING MATRICES:
Gluten (Gliadin competitive ELISA testing)
Dairy, Lactose, & Casein derivatives
Soy protein fractions & Soy lecithin cross-contact
Egg proteins & Albumen residues
Peanuts, Tree Nuts, & Legume derivatives
Wheat, Crustacean Shellfish, & Synthetic binders
Microbes & Toxins
Microbiological controls safeguard your native gut microbiome and overall gut health. We verify every batch to confirm it is entirely free of opportunistic bacteria, dangerous yeasts, and pathogenic molds that trigger immune irritation or compromise capsule shelf-life. Our strict limits shield your system from unwanted biological stress.
MICROBIOLOGICAL PROTOCOLS & DETECTIONS:
Total Aerobic Microbial Count (TAMC) — < 1,000 CFU/g
Total Combined Yeasts and Molds Count (TYMC) — < 100 CFU/g
Salmonella species — Absent in 10g (Zero Tolerance)
Escherichia coli (E. coli) — Absent in 10g (Zero Tolerance)
Whether you are an elite athlete or optimizing your daily routine, chemical safety is vital. Our formulations are structurally screened against product adulteration, unlisted stimulants, and prohibited compounds. We cross-verify our batches against both national FDA regulatory restriction lists and international anti-doping criteria.
This preventative auditing guarantees that our raw active compounds are never mixed, spiked, or altered by unlisted agents during production, giving you absolute confidence in our clean-label purity.
Demystifying the technical markers and clinical metrics behind our testing infrastructure.
Accelerated Stability Testing
A rigorous testing protocol that subjects a formulation to elevated environmental stressors—such as increased temperature and humidity—over a compressed timeline. This process scientifically projects and verifies long-term molecular integrity, potency patterns, and foundational shelf-life stability.
HPTLC
High-Performance Thin-Layer Chromatography: An advanced form of analytical chemistry used for “botanical fingerprinting” to verify the exact species and potency of a plant compound, ensuring complete identity verification before processing.
ICP-MS
Inductively Coupled Plasma Mass Spectrometry: An ultra-sensitive analytical screening method used to isolate and track heavy trace metals down to parts-per-billion (ppb). This guarantees that environmental factors have not altered raw material safety frameworks.
Bioavailability
The measurement tracking how efficiently and completely a targeted molecule passes through standard metabolic pathways to become active inside your cells. High bioavailability means your system safely uses the exact concentration listed.
ELISA Testing
Enzyme-Linked Immunosorbent Assay: A specialized diagnostic processing system that isolates specific proteins. We deploy this validation framework to check for trace cross-reactive food fractions down to exact microscopic boundaries.
TAMC / TYMC
Total Aerobic Microbial Count & Total Combined Yeasts and Molds Count: Crucial structural parameters that set quantitative safety boundaries for biological activity. These thresholds guarantee that standard shelf-life timelines remain clean and stable.
Technical Dossier
A comprehensive, multi-phase document containing deep scientific literature safety justifications, clinical stability reports, and analytical data validation. This official master portfolio is evaluated under strict administrative lenses to secure mandatory product registration nodes.
