1. Home
  2. Labeler Index
  3. An Co Ltd.
  4. NDC Product Code: 69153-110 An Adc Sp Intensive Bb

NDC 69153-110 An Adc Sp Intensive Bb

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69153-110?
  4. An Adc Sp Intensive Bb 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:
69153-110
Proprietary Name:
An Adc Sp Intensive Bb
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
An Co Ltd.
Labeler Code:
69153
Product Label ID:
a2595e72-58f2-4c94-8944-3354a9b2fbaf
Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69153-110-02

Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE (69153-110-01)

Product Details

What is NDC 69153-110?

The NDC code 69153-110 is assigned by the FDA to the product An Adc Sp Intensive Bb 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 69153-110-02 1 tube in 1 carton / 50 g in 1 tube (69153-110-01). 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 Sp Intensive Bb?

This product is used as Purpose: Sunscreen

Which are An Adc Sp Intensive Bb UNII Codes?

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

Which are An Adc Sp Intensive Bb 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".