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  4. NDC Product Code: 16903-168 Theraderm Pain Relieving Patch

NDC 16903-168 Theraderm Pain Relieving Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 16903-168?
  5. Theraderm Pain Relieving Patch 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:
16903-168
Proprietary Name:
Theraderm Pain Relieving Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Manna Omni International Incorporated
Labeler Code:
16903
Product Label ID:
e0e280f4-2c12-4203-be54-c19821b13393
Start Marketing Date: [9]
06-05-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
RECTANGLE (C48347)

Code Structure Chart

Product Details

What is NDC 16903-168?

The NDC code 16903-168 is assigned by the FDA to the product Theraderm Pain Relieving Patch which is product labeled by Manna Omni International Incorporated. The product's dosage form is . The product is distributed in a single package with assigned NDC code 16903-168-01 5 patch in 1 package . 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 Theraderm Pain Relieving Patch?

Adults and children 12 years and over apply to affected area, change patch 2 to 3 times daily.Children under 12 years ask a doctor before use.How to apply:Clean and dry affected area.Cut open poutch and remove patch.If desired, cut patch to size.remove protective film from adhesive, apply directly onto site of pain, and secure ith adhesive strips.

Which are Theraderm Pain Relieving Patch UNII Codes?

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

Which are Theraderm Pain Relieving Patch 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".