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  4. NDC Product Code: 55910-602 Rexall Vanishing Scent Pain Relieving

NDC 55910-602 Rexall Vanishing Scent Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55910-602?
  4. Rexall Vanishing Scent Pain Relieving 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.
NDC Product Code:
55910-602
Proprietary Name:
Rexall Vanishing Scent Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dolgencorp, Llc
Labeler Code:
55910
Product Label ID:
1489dfdd-374e-4b7d-9446-1c5105c7bc5a
Start Marketing Date: [9]
03-14-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 55910-602-04

Package Description: 1 TUBE in 1 CARTON / 57 g in 1 TUBE

Product Details

What is NDC 55910-602?

The NDC code 55910-602 is assigned by the FDA to the product Rexall Vanishing Scent Pain Relieving which is product labeled by Dolgencorp, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55910-602-04 1 tube in 1 carton / 57 g in 1 tube. 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 Rexall Vanishing Scent Pain Relieving?

Uses temporarily relieves the minor aches and pains of muscles and joints associated with - simple backache - atrhritis - strains - bruises - sprains

Which are Rexall Vanishing Scent Pain Relieving UNII Codes?

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

Which are Rexall Vanishing Scent Pain Relieving 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".