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  4. NDC Product Code: 79804-282 Pain Relief Roll On

NDC 79804-282 Pain Relief Roll On

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 79804-282?
  5. Pain Relief Roll On Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
79804-282
Proprietary Name:
Pain Relief Roll On
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Eagle Labs Inc
Labeler Code:
79804
Product Label ID:
2380a400-062a-4a8d-a594-a2e097219044
Start Marketing Date: [9]
11-07-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - SEMI-TRANSLUCENT)

Code Structure Chart

Product Details

What is NDC 79804-282?

The NDC code 79804-282 is assigned by the FDA to the product Pain Relief Roll On which is product labeled by Eagle Labs Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79804-282-03 87 g 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 Pain Relief Roll On?

Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor

Which are Pain Relief Roll On UNII Codes?

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

Which are Pain Relief Roll On 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:

What is the NDC to RxNorm Crosswalk for Pain Relief Roll On?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2610122 - camphor 5 % / capsaicin 0.025 % / menthol 6 % Topical Solution
  • RxCUI: 2610122 - camphor 50 MG/ML / capsaicin 0.25 MG/ML / menthol 60 MG/ML Topical Solution

* Please review the disclaimer below.

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".