NDC 71618-001 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:
71618-001
Proprietary Name:
No Pain More Gain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Compes Cosmetic
Labeler Code:
71618
Start Marketing Date: [9]
07-28-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71618-001-01

Package Description: 100 mg in 1 PACKAGE

Product Details

What is NDC 71618-001?

The NDC code 71618-001 is assigned by the FDA to the product No Pain More Gain which is product labeled by Compes Cosmetic. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71618-001-01 100 mg in 1 package . 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 Gain CreamMoisturizing Pain ReliefNPMG provides temporary but long lasting pain relief and moisturizes the skin. The natural alternative with the advanced German formula starts to work on contact.NPMG is100% vegangluten-freenot tested on animalsmade from spring waterfree of paraben, paraffin and silicone oilNPMG penetrates deeply, absorbs quickly and has a fresh and pleasant scent.Lugus products for the better.Manufactured exclusively for Lugus Group LLC, Cheyenne, WY 82001 Manufactured by Sowell GmbH 65185 Wiesbaden, Germany MADE IN GERMANYNET WT 3.4 fl oz (100 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".