NDC 69739-100 Atobos Centella Baby Aqua Soothing

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:
69739-100
Proprietary Name:
Atobos Centella Baby Aqua Soothing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
1004laboratory
Labeler Code:
69739
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69739-100-01

Package Description: 160 mL in 1 CARTON

Product Details

What is NDC 69739-100?

The NDC code 69739-100 is assigned by the FDA to the product Atobos Centella Baby Aqua Soothing which is product labeled by 1004laboratory. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69739-100-01 160 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 Atobos Centella Baby Aqua Soothing?

Indications & Usage: After washing the face & body, dispense an appropriate amount into your palm, and evenly apply to the entire face and body.

Which are Atobos Centella Baby Aqua Soothing UNII Codes?

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

Which are Atobos Centella Baby Aqua Soothing 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".