NDC 72347-070 Optimal Alcohol Prep Pad

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:
72347-070
Proprietary Name:
Optimal Alcohol Prep Pad
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hilco Vision
Labeler Code:
72347
Start Marketing Date: [9]
02-25-2013
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - PACKET WRAPPER IS WHITE WITH BLUE LETTERING)
Shape:
RECTANGLE (C48347)

Product Packages

NDC Code 72347-070-02

Package Description: 200 PACKET in 1 BOX / 1 g in 1 PACKET (72347-070-01)

NDC Code 72347-070-03

Package Description: 20 BOX in 1 CASE / 200 PACKET in 1 BOX (72347-070-02) / 1 g in 1 PACKET (72347-070-01)

Product Details

What is NDC 72347-070?

The NDC code 72347-070 is assigned by the FDA to the product Optimal Alcohol Prep Pad which is product labeled by Hilco Vision. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 72347-070-02 200 packet in 1 box / 1 g in 1 packet (72347-070-01), 72347-070-03 20 box in 1 case / 200 packet in 1 box (72347-070-02) / 1 g in 1 packet (72347-070-01). 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 Optimal Alcohol Prep Pad?

Apply topically as needed to cleanse

Which are Optimal Alcohol Prep Pad UNII Codes?

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

Which are Optimal Alcohol Prep Pad 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 Optimal Alcohol Prep Pad?

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:

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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".