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  4. NDC Product Code: 72895-001 Deep Muscle Rub

NDC 72895-001 Deep Muscle Rub

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72895-001?
  4. Deep Muscle Rub 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:
72895-001
Proprietary Name:
Deep Muscle Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laiden Montana Emu Products
Labeler Code:
72895
Product Label ID:
8038f2e0-7683-6be4-e053-2a91aa0a9643
Start Marketing Date: [9]
01-24-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 72895-001?

The NDC code 72895-001 is assigned by the FDA to the product Deep Muscle Rub which is product labeled by Laiden Montana Emu Products. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 72895-001-02 60 ml in 1 jar , 72895-001-04 120 ml in 1 jar , 72895-001-08 240 ml in 1 jar , 72895-001-25 7 ml in 1 jar . 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 Deep Muscle Rub?

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.massage into area until thoroughly absorbedChildren under 2 years of age: consult a doctor.

Which are Deep Muscle Rub UNII Codes?

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

Which are Deep Muscle Rub 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".