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  4. NDC Product Code: 51068-507 Activon Ultra Strength Arthritis

NDC 51068-507 Activon Ultra Strength Arthritis

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51068-507?
  4. Activon Ultra Strength Arthritis 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:
51068-507
Proprietary Name:
Activon Ultra Strength Arthritis
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Family First Pharmaceuticals, Inc.
Labeler Code:
51068
Product Label ID:
09d6b5a1-9223-4b60-b92d-7883a434a13e
Start Marketing Date: [9]
02-15-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51068-507-01

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

Product Details

What is NDC 51068-507?

The NDC code 51068-507 is assigned by the FDA to the product Activon Ultra Strength Arthritis which is product labeled by Family First Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51068-507-01 1 canister in 1 carton / 57 g in 1 canister. 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 Activon Ultra Strength Arthritis?

Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily.children under 12 years of age: ask a doctor

Which are Activon Ultra Strength Arthritis UNII Codes?

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

  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)

Which are Activon Ultra Strength Arthritis 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 Activon Ultra Strength Arthritis?

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:

* Please review the disclaimer below.

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".