NDC 70984-001 Raging Kakapo Pain Relieve

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:
70984-001
Proprietary Name:
Raging Kakapo Pain Relieve
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Effihealth Llc
Labeler Code:
70984
Start Marketing Date: [9]
10-25-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70984-001-01

Package Description: 1 JAR in 1 CARTON / 113.4 g in 1 JAR

Product Details

What is NDC 70984-001?

The NDC code 70984-001 is assigned by the FDA to the product Raging Kakapo Pain Relieve which is product labeled by Effihealth Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70984-001-01 1 jar in 1 carton / 113.4 g 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 Raging Kakapo Pain Relieve?

This product is used as Active IngredientsPurposeCapsaicin 0.025%Topical AnalgesicHistamine Dihydrochloride 0.075%Topical Analgesic. For the temporary relief of minor aches and pains of muscles and joints associated witharthritissimple backachestrainsbruises and sprains.

Which are Raging Kakapo Pain Relieve UNII Codes?

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

Which are Raging Kakapo Pain Relieve 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 Raging Kakapo Pain Relieve?

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: 1986870 - capsaicin 0.025 % / histamine dihydrochloride 0.075 % Topical Cream
  • RxCUI: 1986870 - capsaicin 0.25 MG/ML / histamine dihydrochloride 0.75 MG/ML Topical Cream

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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".