NDC 71969-111 Diaper

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:
71969-111
Proprietary Name:
Diaper
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medek Laboratories Inc.
Labeler Code:
71969
Start Marketing Date: [9]
03-08-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71969-111-01

Package Description: 170 g in 1 JAR

NDC Code 71969-111-02

Package Description: 1 TUBE in 1 PACKAGE / 57 g in 1 TUBE

Product Details

What is NDC 71969-111?

The NDC code 71969-111 is assigned by the FDA to the product Diaper which is product labeled by Medek Laboratories Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71969-111-01 170 g in 1 jar , 71969-111-02 1 tube in 1 package / 57 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 Diaper?

UsesHelp heal and prevent diaper rashProtects chafed skin due to diaper rash and helps protect wetness

Which are Diaper UNII Codes?

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

Which are Diaper 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".