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  4. NDC Product Code: 69650-001 Capment

NDC 69650-001 Capment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69650-001?
  4. Capment 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:
69650-001
Proprietary Name:
Capment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Original Patch Company Inc
Labeler Code:
69650
Product Label ID:
809f0f24-5a4c-451a-9528-e2250a483e8f
Start Marketing Date: [9]
03-24-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69650-001?

The NDC code 69650-001 is assigned by the FDA to the product Capment which is product labeled by Original Patch Company Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69650-001-15 15 patch in 1 box / 1 g in 1 patch (69650-001-05). 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 Capment?

Adults and children 12 and over: Apply patch to affected area 1 to 2 times daily or as directed.Instructions for Use:Clean and dry affected areaOpen pouch and remove on patchRemove any protective film and apply directly to affected area of painWash hands with soap and water after applying patchReseal pouch containing unused patches after each use

Which are Capment UNII Codes?

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

Which are Capment 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:

  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H)

* 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.

[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".