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  4. NDC Product Code: 69161-007 No Pain More Gain

NDC 69161-007 No Pain More Gain

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69161-007?
  4. No Pain More Gain Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 69161-007 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
69161-007
Proprietary Name:
No Pain More Gain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lugus Group Llc
Labeler Code:
69161
Product Label ID:
66b5b550-c4ee-5bb5-e053-2991aa0a36dc
FDA Application Number: [6]
part348
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69161-007?

The NDC code 69161-007 is assigned by the FDA to the product No Pain More Gain which is product labeled by Lugus Group Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69161-007-01 150 mg in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for No Pain More Gain?

No Pain More GainSport StrengthPre & Post Workout100% Vegan No Animal TestingNPMG is • 100% vegan • Gluten-free • GMO-free • Free of paraben, paraffin and silicone oil • Made from spring water • Cruelty-freeBuild muscle and get strong faster. NPMG Sport Strength is a superior pre-and post-workout spray optimized for bodybuilding and all strength related sports, endorsed by physiotherapists. The innovative crackling spray contains tiny bubbles. They burst on contact with the skin and release their unique properties. NPMG Sport Strength is cold at first, then warm. It can be used selectively, but also on large areas. It is made from the finest spring water. Its proprietary blend is loaded with minerals and electrolytes, powered by menthol, enhanced by colloidal gold and optimized with lemon and almond oil. NPMG Sport Strength penetrates deeply, absorbs quickly, moisturizes the skin and has a fresh and pleasant scent.The natural alternative with the advanced German formula starts to work on contact, penetrates deeply, absorbs quickly and has a fresh and pleasant scent.NPMG Sport Strength is a product ofLugus Group LLC, Buffalo, WY 82834, USANET WT 5.07 fl oz (150 ml)

Which are No Pain More Gain UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are No Pain More Gain Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".