NDC 72895-081 Banish My Pain

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:
72895-081
Proprietary Name:
Banish My Pain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laiden Montana Emu Products
Labeler Code:
72895
Start Marketing Date: [9]
05-06-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72895-081-02

Package Description: 60 mL in 1 JAR

Product Details

What is NDC 72895-081?

The NDC code 72895-081 is assigned by the FDA to the product Banish My Pain which is product labeled by Laiden Montana Emu Products. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72895-081-02 60 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 Banish My Pain?

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 Banish My Pain UNII Codes?

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

Which are Banish My Pain 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".