NDC 71638-0006 Pick Me Pad Azulene Moisture

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:
71638-0006
Proprietary Name:
Pick Me Pad Azulene Moisture
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dermafirm Inc.
Labeler Code:
71638
Start Marketing Date: [9]
09-04-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71638-0006-1

Package Description: 110 g in 1 BOTTLE

Product Details

What is NDC 71638-0006?

The NDC code 71638-0006 is assigned by the FDA to the product Pick Me Pad Azulene Moisture which is product labeled by Dermafirm Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71638-0006-1 110 g in 1 bottle . 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 Pick Me Pad Azulene Moisture?

After cleansing, gently wipe the entire face with the soft side of the pattern, and gently wipe in the direction of skin texture.You can also patch it like a facial pack in the dry areas. Close the cap tightly to prevent the pad from drying.

Which are Pick Me Pad Azulene Moisture UNII Codes?

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

Which are Pick Me Pad Azulene Moisture 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".