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  4. NDC Product Code: 64479-200 Painpatrol Professional Pain Relief

NDC 64479-200 Painpatrol Professional Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64479-200?
  4. Painpatrol Professional Pain Relief 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:
64479-200
Proprietary Name:
Painpatrol Professional Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Smartscience Laboratories, Inc.
Labeler Code:
64479
Product Label ID:
930840a7-4a41-4c8a-a9d0-72b400ed2a03
Start Marketing Date: [9]
03-10-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64479-200-10

Package Description: 88 mL in 1 BOTTLE, WITH APPLICATOR

NDC Code 64479-200-12

Package Description: 944 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 64479-200?

The NDC code 64479-200 is assigned by the FDA to the product Painpatrol Professional Pain Relief which is product labeled by Smartscience Laboratories, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 64479-200-10 88 ml in 1 bottle, with applicator , 64479-200-12 944 ml in 1 bottle, pump . 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 Painpatrol Professional Pain Relief?

Use only as directedDo not use on children under 12 years of age.Roll onto affected area no more than four times daily. Shake well before each use.

Which are Painpatrol Professional Pain Relief 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 Painpatrol Professional Pain Relief 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 Painpatrol Professional Pain Relief?

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:

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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".