NDC 11777-001 Nmnpqq

Nmnpqq

NDC Product Code 11777-001

NDC 11777-001-01

Package Description: 60 CAPSULE in 1 PACKAGE > 1 mg in 1 CAPSULE

NDC Product Information

Nmnpqq with NDC 11777-001 is a a human over the counter drug product labeled by Golden Life Health Products Limited. The generic name of Nmnpqq is nmnpqq. The product's dosage form is powder and is administered via topical form.

Labeler Name: Golden Life Health Products Limited

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Nmnpqq Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • PYRROLOQUINOLINEDIONE TRICARBOXYLIC ACID 10 mg/100mg
  • NICOTINAMIDE RIBOTIDE 45 mg/100mg

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • RESVERATROL (UNII: Q369O8926L)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Golden Life Health Products Limited
Labeler Code: 11777
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 12-23-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Nmnpqq Product Label Images

Nmnpqq Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Dosage & Administration

Serving Two capsule per day after meal.

Usual adult usage: Six capsules maximum in 24 hours ifneeded. Do not exceed the limitation.

Information

Keep tightly closed, Protect from light.

Store at Refrigerator is recommended. Store at controlled room temperature between 20℃ to 25 ℃ celsius or 68°F to 77°F Fahrenheit

Indications & Usage

This product is not recommended for cancer patients,pregnant women, and people age below 18 years oldbased on scientific research. lf you have any questions,please consult doctors or professionals for more information.

Inactive Ingredient

Resveraltrol

Otc - Active Ingredient

Nicotinamide mononucleotide 200mg 45%pyrroloquinoline quinone 50mg 10%

Otc - Keep Out Of Reach Of Children

Keep out of children's reach.

Otc - Purpose

Every capsule contains

200mg Nicotinamide Mononucleotide for NAD+ Support.

50mg Pyrroloquinoline Quinone Enzymefor Mitochondrion Support

Warnings

Sealed for safety and freshness free of artificial colors,preservatives , or sweeteners, No dairy, starch, wheat,gluten, yeast, soil, corn, egg tree nuts, or GMOs.

* Please review the disclaimer below.