NDC 73417-852 Totalarthritis

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:
73417-852
Proprietary Name:
Totalarthritis
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Phytobiologic Pharmaceutics Llc
Labeler Code:
73417
Start Marketing Date: [9]
08-12-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73417-852-52

Package Description: 1 JAR in 1 CARTON / 25 g in 1 JAR

Product Details

What is NDC 73417-852?

The NDC code 73417-852 is assigned by the FDA to the product Totalarthritis which is product labeled by Phytobiologic Pharmaceutics Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73417-852-52 1 jar in 1 carton / 25 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 Totalarthritis?

Apply a generous amount of the ointment (~1g) on affected area 4 times daily and massage gently. For faster results, applylocal heat with a heat lamp or heat pad after each application.For chronic severe conditions, use the ointment for 6 to 9 months and as advised by the physician*.* Individual results vary depending on the chronic conditions, age and time length of suffering.

What is the NDC to RxNorm Crosswalk for Totalarthritis?

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: 2566038 - camphor 4 % / eugenol 4 % / menthol 4 % Topical Ointment
  • RxCUI: 2566038 - camphor 0.04 MG/MG / eugenol 0.04 MG/MG / menthol 0.04 MG/MG Topical Ointment

* 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".