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  4. NDC Product Code: 69788-001 Eczema

NDC 69788-001 Eczema

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69788-001?
  4. Eczema Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69788-001
Proprietary Name:
Eczema
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Moogoo Usa Llc
Labeler Code:
69788
Product Label ID:
82bc158e-c692-4cc9-9967-2eb29cee7226
Start Marketing Date: [9]
04-05-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 69788-001?

The NDC code 69788-001 is assigned by the FDA to the product Eczema which is product labeled by Moogoo Usa Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69788-001-01 100 g in 1 package . 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 Eczema?

Eczema CreamSkin Protectant with Colloidal OatmealMooGooFor Symptomatic Relief of Eczema (Atopic Dermatitis)Finally, an alternative!Eczema is very common in children and some adults. Our website has more information on how to manage this condition.MooGoo products originate from a cream used in australian dairy farms to repair the skin on cow's udders! This cream was full of natural skin healing ingredients, and no gimmicks. All MooGoo products are made this way.

Which are Eczema UNII Codes?

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

Which are Eczema 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:

What is the NDC to RxNorm Crosswalk for Eczema?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* 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".