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  4. NDC Product Code: 71955-100 Ageranium Patch

NDC 71955-100 Ageranium Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71955-100?
  4. Ageranium Patch 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:
71955-100
Proprietary Name:
Ageranium Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Entom Co., Ltd.
Labeler Code:
71955
Product Label ID:
6182bea6-1606-c6f9-e053-2a91aa0a5f51
Start Marketing Date: [9]
12-29-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71955-100-02

Package Description: 8 POUCH in 1 BOX / 4 PATCH in 1 POUCH (71955-100-01) / 99.13 mg in 1 PATCH (71955-100-00)

Product Details

What is NDC 71955-100?

The NDC code 71955-100 is assigned by the FDA to the product Ageranium Patch which is product labeled by Entom Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71955-100-02 8 pouch in 1 box / 4 patch in 1 pouch (71955-100-01) / 99.13 mg in 1 patch (71955-100-00). 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 Ageranium Patch?

Adults and children over 12 years of age- clean and dry affected area- remove patch from film- remove patch slowly and gentle from the skin after at most 8 hours applicationChildren under 12 years of age:consult a doctor

Which are Ageranium Patch UNII Codes?

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

Which are Ageranium 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:

* 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".