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  4. NDC Product Code: 11344-003 50% Rubbing

NDC 11344-003 50% Rubbing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11344-003?
  4. 50% Rubbing Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
11344-003
Proprietary Name:
50% Rubbing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sound Body
Labeler Code:
11344
Product Label ID:
cea74c5e-ef73-473d-bdd0-449394f798a1
Start Marketing Date: [9]
10-08-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 11344-003?

The NDC code 11344-003 is assigned by the FDA to the product 50% Rubbing which is product labeled by Sound Body. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 11344-003-43 473 ml in 1 bottle, plastic , 11344-003-45 946 ml in 1 bottle, plastic . 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 50% Rubbing?

Clean the affected areaapply a small amount of the is product on the affected area 1 to 3 times dailymay be covered with a sterile bandateif bandaged, let dry first

Which are 50% Rubbing UNII Codes?

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

Which are 50% Rubbing 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 50% Rubbing?

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:

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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".