NDC 67151-303 Wipes Plus

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:
67151-303
Proprietary Name:
Wipes Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
67151
Start Marketing Date: [9]
09-04-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 67151-303?

The NDC code 67151-303 is assigned by the FDA to the product Wipes Plus which is product labeled by Progressive Products, Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 67151-303-01 80 swab in 1 package , 67151-303-04 240 swab in 1 bottle , 67151-303-07 800 swab in 1 bottle , 67151-303-08 1200 swab in 1 bottle , 67151-303-09 1500 swab 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 Wipes Plus?

Remove lid.Pull wipe from enter of roll and thread through opening lid. Do not push finger through oepning.Replace lid, pull wipe up, and then out at 45 angle.The next wipe dispenses automatically.Close lid to retain moisture.

Which are Wipes Plus UNII Codes?

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

Which are Wipes Plus 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 Wipes Plus?

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".