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  4. NDC Product Code: 51985-010 Iontophoresis Anti Aging Solution I

NDC 51985-010 Iontophoresis Anti Aging Solution I

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51985-010?
  4. Iontophoresis Anti Aging Solution I 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:
51985-010
Proprietary Name:
Iontophoresis Anti Aging Solution I
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rocket Electric Co., Ltd.
Labeler Code:
51985
Product Label ID:
13819a55-92e5-4c24-8d2c-43df3c500092
Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51985-010-01

Package Description: 20 mL in 1 CARTON

Product Details

What is NDC 51985-010?

The NDC code 51985-010 is assigned by the FDA to the product Iontophoresis Anti Aging Solution I which is product labeled by Rocket Electric Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51985-010-01 20 ml in 1 carton . 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 Iontophoresis Anti Aging Solution I?

Directions:Apply Anti aging serum and pat gently for about a minute.Peel patch from liner and turn over. black side onto skin.Place patch around eye and leave on for 1 hour then remove.

Which are Iontophoresis Anti Aging Solution I UNII Codes?

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

Which are Iontophoresis Anti Aging Solution I 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".