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  4. NDC Product Code: 63029-062 Goodys Pm Pain Reliever

NDC 63029-062 Goodys Pm Pain Reliever

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63029-062?
  5. Goodys Pm Pain Reliever Uses
  6. Active Ingredients UNII Codes
  7. 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:
63029-062
Proprietary Name:
Goodys Pm Pain Reliever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medtech Products Inc.
Labeler Code:
63029
Product Label ID:
8d4fc971-492d-471d-a3c2-7d8e2237a5f3
Start Marketing Date: [9]
07-13-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
17 MM
Imprint(s):
2793
Score:
1

Code Structure Chart

Product Details

What is NDC 63029-062?

The NDC code 63029-062 is assigned by the FDA to the product Goodys Pm Pain Reliever which is product labeled by Medtech Products Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63029-062-10 1 bottle in 1 carton / 100 capsule, coated in 1 bottle, 63029-062-24 1 bottle in 1 box / 24 capsule, coated in 1 bottle. 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 Goodys Pm Pain Reliever?

Do not take more than directed (see overdose warning)drink a full glass of water with each doseadults and children 12 years and over: take 2 caplets every 6 hours; not more than 8 caplets in 24 hourschildren under 12 years of age: ask a doctor

Which are Goodys Pm Pain Reliever UNII Codes?

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

Which are Goodys Pm Pain Reliever 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".