NDC 63940-802 Harmon Face Values Medicated Wipes

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:
63940-802
Proprietary Name:
Harmon Face Values Medicated Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Harmon Stores Inc.
Labeler Code:
63940
Start Marketing Date: [9]
07-31-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63940-802-48

Package Description: 48 CLOTH in 1 POUCH

Product Details

What is NDC 63940-802?

The NDC code 63940-802 is assigned by the FDA to the product Harmon Face Values Medicated Wipes which is product labeled by Harmon Stores Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63940-802-48 48 cloth in 1 pouch . 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 Harmon Face Values Medicated Wipes?

DirectionsAdults and children 12 years and older- Up to 6 times daily or after each bowel movementChildren under 12- Consult a doctorWhen practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.Gently dry by patting or blotting with toilet tissue or soft cloth before each application of this product.  Gently apply to the affected area by patting and discard.  Apply to the affected area up to 6 times daily or after each bowel movement.

Which are Harmon Face Values Medicated Wipes UNII Codes?

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

Which are Harmon Face Values Medicated Wipes 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".