The only NMN in the world to achieve 11 certifications
iHealth's NMN is the first NMN product in the world to be included in the Physician Desk References (PDR), making it the safest and most effective product of its kind! This is one of the very few NMN products with complete and clear details, representing 100% responsibility to consumers.
The only NMN brand in the U.S. that has obtained ConsumerLab Qquality Certificate
iHealth's NMN is the first NMN product in the USA to obtained ConsumerLab Quality Certificate
The first NMN brand to obtain FDA Certificate of Free Sale
iHealth's NMN is the first NMN product to obatain FDA Certificate of Free Sale
NMN brand that obtained Health Certificate
iHealth's NMN is the NMN product to obatain Health Certificate and legally shipped to China through bonded warehouses.
How to choose NMN?
The purity, manufacturing process, grade and content of NMN are the most important criteria to judge.
NMN Production Technology
The production technology of NMN can be the main reason that affects the quality and price of the product.
Chemically synthesized NMN is cheap because of its low cost.
The price of yeast fermentation NMN is the highest, and the unit price of one bottle of NMN may be more than $2,500 USD.
Biological enzyme method NMN has the best balance of quality and price.
iHealth's NMN is made by the biological enzyme method, and it is a laboratory-grade NMN, which is definitely the most stringent in the industry in terms of quality!
The Importance of Authoritative Certification
When it comes to choosing health products, the only way to prove the safety and effectiveness of a product is to have it certified by a third-party authority!
iHealth's NMN is the only NMN in the world that has been certified by nine authoritative organizations, which is the best in the industry in terms of safety and effectiveness.
Why choose iHealth's NMN?
iHealth's NMN is the only NMN in the world that has obtained 11 major certifications, leading the health industry in terms of safety and effectiveness!
The Physician’s Desk Reference, PDR, is the most authoritative doctor’s drug collection in the United States. All prescription drugs must be certified and approved by the FDA (Food and Drug Administration). Under each drug item, the prescription specifications of the drug are included. Basic excipients, instructions for use, pharmacology, and clinical applications are very detailed. Physicians rely on it to accurately query drug information, prescribe more accurately, ensure medication safety. In addition to collecting drug information, PDR also publishes information on nutrient supplements and over-the-counter drugs that meet safety requirements.
PDR distributes product information to doctors, pharmacists, and other healthcare providers in the United States, as well as hospitals and medical education institutions through a variety of channels.
FDA Certificate of Free Sale
US Food and Drug Administration (FDA) is a federal government agency directly under the jurisdiction of the US Department of Health and Human Services. Its primary function is to be responsible for the production, importation of food, dietary supplements, and pharmaceuticals in the United States. It provides supervision and management of vaccines, biomedical preparations, blood preparations, medical equipment, radioactive equipment, veterinary drugs and cosmetics.
It is the legal standard for the production of food, nutritional supplements and pharmaceuticals in the United States. The specific criteria for cGMP are based on the specific product type. Its contents include plant construction, personnel requirements, sanitary conditions, and production, quality management and records. The supervision and implementation of this standard is performed by the FDA.
cGMP refers to dynamic pharmaceutical production management practices and is also translated into current pharmaceutical production management practices. It requires verification throughout the entire production and logistics process. cGMP is an international pharmaceutical production management standard.
Consumer labs have perhaps the highest testing standards among third-party certifiers for dietary supplements, and are the only ones that publicly publish their testing methods and quality standards.
This logo is created and managed by a vegetarian organization. It is a simple and easily recognizable logo. It tells you the products not contain any animal ingredients, such as health products, foods, clothing, cosmetics, and etc.
Halal Certificate is a qualification certificate issued after the certification of food, medicine, chemicals, and additives in accordance with Muslim customs. This is a process in which a qualified independent third party supervises consumer products to ensure products produced demonstrate and meet the production readiness and ingredient standards of the halal lifestyle. When the supervisory third party successfully passes and accepts the product, a halal certification is issued to the manufacturer to confirm that the product is halal. Although halal requires food to be hygienic and pure, halal certification is handed over to government regulators for food safety issues.
UL is a shorthand for Underwriters Laboratories Inc. The UL Safety Laboratory is the most authoritative in the United States and the largest private institution in the world for safety testing and identification. It is an independent, profitable, professional organization that tests for public safety. It uses scientific testing methods to determine the extent to which various materials, devices, products, equipment, and buildings are hazardous or harmful to life and property; to determine, prepare, and issue appropriate standards and to help reduce and prevent life. UL certification is a non-mandatory certification in the United States, primarily for the detection and certification of product safety performance. UL plays an active role in promoting the development of international trade.
Hazard Analysis Critical Control Point is a scientific, simple and practical preventive food safety control system. It is based on GMP (Good Manufacturing Practice) and SSOP (Sanitary Standard Operating Procedure). One of the most effective means of self-control of food safety. Since the HACCP system appeared in the United States in the 1960s and became the first in some areas in the 1990s, it has attracted widespread international attention and recognition. The government authorities in some countries have also developed GMP and regulations for their food industry. There are mandatory requirements for the safety and health control of food enterprises in the country and the exporting country.
HACCP is recognized worldwide for its ability to significantly reduce the risk of food safety hazards. HACCP system validation and certification helps to build public confidence.
Material Safety Data Sheet
MSDS is a comprehensive document that manufacturers provide customers with detailed information on the toxicity, environmental hazards, and safe use of substances to help customers control risks.
For a product to be kosher certified, and to qualify for a kosher certificate, each ingredient, food additive and processing aid used in its production must also be kosher. The production process must be suitable for kosher requirements and therefore it must be approved by a kosher auditor.
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