NDC 69153-020 An Adc Face Up Special Program

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
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
Start Marketing Date: [9]
08-01-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69153-020-01

Package Description: 10 SOLUTION in 1 CARTON

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.

[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".