NDC 81816-001 Neolinn

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:
81816-001
Proprietary Name:
Neolinn
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Remy Biosciences, Inc.
Labeler Code:
81816
Start Marketing Date: [9]
04-30-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81816-001-30

Package Description: 30 POUCH in 1 BOX / 1 PATCH in 1 POUCH (81816-001-01) / 300 mg in 1 PATCH

Product Details

What is NDC 81816-001?

The NDC code 81816-001 is assigned by the FDA to the product Neolinn which is product labeled by Remy Biosciences, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81816-001-30 30 pouch in 1 box / 1 patch in 1 pouch (81816-001-01) / 300 mg in 1 patch. 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 Neolinn?

Uses:Temporarily relieves minor aches and muscle pains associated witharthritis, simple backache, strains, muscle soreness and stiffness.

Which are Neolinn UNII Codes?

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

Which are Neolinn 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:

  • CANNABIDIOL (UNII: 19GBJ60SN5)
  • DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • TRIMETHYLSILYL TREATED DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (45/55 W/W; 100000 PA.S) (UNII: 5VBE2X0WG0)
  • TRIMETHYLSILYL TREATED DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 5000000 PA.S) (UNII: 9N5G1G3D3H)

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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".