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  4. NDC Product Code: 66007-145 Junior Strength Pain Relief

NDC 66007-145 Junior Strength Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66007-145?
  5. Junior Strength Pain Relief Uses
  6. Active 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.

Get all the details for National Drug Code (NDC) 66007-145 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
66007-145
Proprietary Name:
Junior Strength Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Capricorn Pharma Inc.
Labeler Code:
66007
Product Label ID:
9fa0eaa3-d9c6-45c8-9613-edf9e50021e9
FDA Application Number: [6]
part343
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date: [9]
07-26-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - LIGHT PURPLE/VIOLET)
Shape:
ROUND (C48348)
Size(s):
14 MM
Imprint(s):
CP
Score:
2
Flavor(s):
GRAPE (C73391)

Code Structure Chart

Product Details

What is NDC 66007-145?

The NDC code 66007-145 is assigned by the FDA to the product Junior Strength Pain Relief which is product labeled by Capricorn Pharma Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66007-145-02 4 blister pack in 1 carton / 6 tablet in 1 blister pack (66007-145-01). 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 Junior Strength Pain Relief?

This product does not contain directions or complete warnings for adult use.Do not exceed recommended dose (see overdose warning)■ find right dose on chart below. If possible, use weight to dose; otherwise, use age■ dissolve in mouth or chew before swallowing■ if needed, repeat dose every 4 hours ■ do not use more than 5 times in 24 hoursWeight (lb)Under 4848-5960-7172-9596 and overAge (yr)Under 66-89-101112TabletsAsk a doctor22-1/234

Which are Junior Strength Pain Relief UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Junior Strength 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:

* 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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".