NDC 71637-003 No Pain More Gain

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71637-003
Proprietary Name:
No Pain More Gain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
71637
Start Marketing Date: [9]
03-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71637-003?

The NDC code 71637-003 is assigned by the FDA to the product No Pain More Gain which is product labeled by Vema Industrie-verpackung Gmbh & Co. Kg. Kontrakt - Abfullung Und -verpackung. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71637-003-01 150 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?

100% VeganNo Pain More GainIce SprayMoisturizing Pain ReliefNPMG is • 100% vegan • Gluten-free • Free of paraben, paraffin and silicone oil • Made from spring water • Not tested on animalsFor local inflammatory and noninflammatory pain. No Pain More Gain (NPMG) provides temporary but long lasting pain relief and moisturizes the skin. The innovative crackling spray contains tiny bubbles. On contact with the skin they burst and release their unique pain relieving properties. NPMG Ice Spray is cold at first, then warm. It can be used selectively, but also on large areas. The natural alternative with the advanced German formula starts to work on contact. NPMG penetrates deeply, absorbs quickly and has a fresh and pleasant scent.Lugus 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.

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".