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NDC 69153-020 An Adc Face Up Special Program

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69153-020?
  4. An Adc Face Up Special Program 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.

Get all the details for National Drug Code (NDC) 69153-020 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
69153-020
Proprietary Name:
An Adc Face Up Special Program
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
An Co Ltd.
Labeler Code:
69153
Product Label ID:
ae97e7e4-8c9f-4aa3-9515-ae0037721f98
FDA Application Number: [6]
part347
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date: [9]
08-01-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69153-020?

The NDC code 69153-020 is assigned by the FDA to the product An Adc Face Up Special Program which is product labeled by An Co Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69153-020-01 10 solution 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 An Adc Face Up Special Program?

Indications & usage:1. Open the wine colored pack to the dotted line(please be careful not to spill any of the liquid inside)2. Open the small transparent vial and pour it into the pack (please be careful not to spill)3. Seal the wine colored pack tightly and shake it steadily but vigorously 10 or more times (after shaking adequately the contents should turn into gel).4. Apply the gel mixture all over the face with the included cosmetic brush.5. It may depend on the person, but the wait time is around 15-20 minutes (while waiting, fan your face lightly). Please refrain from moving or speaking as much as possible.6. The first few times the pack may pull very tightly and become discolored depending on the area (due to removing the wastes from inside the skin). The state of being pulled very taut does depend on the skin type, but there is nothing to worry about as the tightening is part of the process.7. After the pack is sufficiently dry, wash it off with warm water; wash twice with soap once again like step number 1 of 1.8. Dab away the excess moisture with a dry towel.

Which are An Adc Face Up Special Program UNII Codes?

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

Which are An Adc Face Up Special Program 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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".