Is Your Sanitary Pad Safe? A Guide to Understanding Certifications & Reading SGS Reports
As women’s health awareness continues to rise globally, the primary criteria for choosing sanitary pads have shifted. Consumers are moving beyond just “absorption capacity” and “price” to prioritize “material safety” and “health benefits.” However, amidst a market flooded with various brands and claims, a common confusion remains: Who defines what is truly “safe”? And how should one interpret complex certification marks and laboratory reports?
As a brand deeply rooted in the feminine hygiene sector, Niceday believes that transparency is the foundation of trust. Today, we are breaking down the “safety code” of sanitary pads from the perspective of professional manufacturing and quality control.
1. Material Safety: Eliminating Risks at the Source
“Is the material in my sanitary pad safe?” This is one of the most frequently asked questions we receive.
The safety of a premium sanitary pad begins with the global sourcing of raw materials. Safety risks often stem from the use of inferior recycled fluff pulp (which may contain fluorescent whitening agents) or Super Absorbent Polymers (SAP) from unknown sources. Truly safe products establish strict barriers within the supply chain.
At Niceday, our production standards mandate the use of raw materials that have undergone rigorous safety assessments. By utilizing high-quality dust-free paper, breathable bottom films, and imported high-efficiency absorbent factors, we ensure not only physical dryness but also chemical safety—strictly eliminating the risk of migratable fluorescent substances, formaldehyde, and heavy metal residues.
2. Choosing Certifications: Authority Matters
Many brands display various certificates, but for B2B buyers and consumers alike, the authority of the issuer matters more than the certificate itself. When evaluating a partner or product, focus on these three categories of authoritative bodies:
Regulatory Certifications (Market Access):
FDA (U.S. Food and Drug Administration): The global benchmark for strict standards. FDA registration signifies that the production facilities and processes meet the hygiene requirements for medical devices in the United States.
CE (Conformité Européenne): The mandatory passport for the European market, indicating the product complies with EU health, safety, and environmental protection standards.
System Certifications (Management Capability):
ISO 9001 / ISO 13485: These are not just pieces of paper; they prove a factory operates under a standardized Quality Management System. ISO 13485 is particularly critical as it represents the standard for medical devices, meaning the enterprise produces sanitary pads with the same rigor used for medical products.
Third-Party Testing (Objective Data):
SGS / Intertek: These internationally recognized testing agencies are known for their independence and impartiality. Their reports do not favor any brand; they let the data speak for itself.
3. Flexible Customization for Your Brand
Whether you are an established brand looking to expand your SKU list or a startup launching a niche product, Niceday offers flexible MOQ and diverse raw material options. We don’t just manufacture; we consult. We help you choose the right SAP (Super Absorbent Polymer) ratio and the perfect packaging design to communicate “Professional Protection” to your end-users.
Build Your "Invisible Armor" Line Today
3. Interpreting Reports: How to Read a Lab Test Like an Expert
Once you have an SGS or Intertek report in hand, where should you look amidst the pages of data? Here are the three core dimensions to focus on:
- Microbiological Indicators (The Hygiene “Red Line”) This is the most basic yet critical section. Look for “Total Bacterial Count” and “Total Fungal Count.”
The Standard: Premium products should show results as “Not Detected” or figures significantly below national/international limits. This directly correlates to preventing infections during menstruation.
- Toxicological Indicators (Chemical Safety) Focus on the test results for “Migratable Fluorescent Substances” and “Formaldehyde.”
Key Point: For any safe product, especially those claiming to be natural (like the Niceday Herbal series), this section must result in “Pass” or “Not Detected.” Zero tolerance for harmful chemical additives is our baseline.
- Performance Indicators (User Experience) While this relates to experience rather than direct safety, it indicates manufacturing quality. Check the “Absorption Ratio” and “Rewet Quantity.”
Data Meaning: A high absorption ratio combined with low rewet quantity means the product locks in liquid quickly and keeps the surface dry. This minimizes the damp environment where bacteria thrive, indirectly protecting intimate health.
Conclusion: Making Safety Visible
At Niceday, we treat safety as a visible commitment. from achieving FDA and CE compliance to the proactive testing of every production batch, we are dedicated to eliminating the information gap. We want our global partners and consumers to feel the warmth and quality of our products through these rigorous reports.
Choosing a sanitary pad is choosing a healthy lifestyle. By understanding certifications and reading reports, you can make every choice with complete peace of mind.
