1. Home
  2. Labeler Index
  3. Laorganic Co., Ltd.
  4. NDC Product Code: 70993-0003 Atono2 Baby Sun Cream

NDC 70993-0003 Atono2 Baby Sun Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70993-0003?
  4. Atono2 Baby Sun Cream 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:
70993-0003
Proprietary Name:
Atono2 Baby Sun Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laorganic Co., Ltd.
Labeler Code:
70993
Product Label ID:
3eb67c20-a1b6-3014-e054-00144ff8d46c
Start Marketing Date: [9]
09-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70993-0003-1

Package Description: 50 g in 1 TUBE

Product Details

What is NDC 70993-0003?

The NDC code 70993-0003 is assigned by the FDA to the product Atono2 Baby Sun Cream which is product labeled by Laorganic Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70993-0003-1 50 g in 1 tube . 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 Atono2 Baby Sun Cream?

Apply proper amount to the skin

Which are Atono2 Baby Sun Cream UNII Codes?

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

Which are Atono2 Baby Sun Cream 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".