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  4. NDC Product Code: 73316-100 Two Old Goats Arthritis Formula Topical Analgesic

NDC 73316-100 Two Old Goats Arthritis Formula Topical Analgesic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73316-100?
  4. Two Old Goats Arthritis Formula Topical Analgesic 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:
73316-100
Proprietary Name:
Two Old Goats Arthritis Formula Topical Analgesic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Two Old Goats
Labeler Code:
73316
Product Label ID:
b017007c-a3f6-5b11-e053-2a95a90ae8bb
Start Marketing Date: [9]
08-12-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73316-100-06

Package Description: 177 mL in 1 TUBE

Product Details

What is NDC 73316-100?

The NDC code 73316-100 is assigned by the FDA to the product Two Old Goats Arthritis Formula Topical Analgesic which is product labeled by Two Old Goats. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73316-100-06 177 ml in 1 tube . 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 Two Old Goats Arthritis Formula Topical Analgesic?

Adults and children 2 years of age and older: Apply to affected area not more than 4 times dailyChildren under 2 years of age: Consulkt a doctor.

Which are Two Old Goats Arthritis Formula Topical Analgesic UNII Codes?

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

Which are Two Old Goats Arthritis Formula Topical Analgesic 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".