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  4. NDC Product Code: 81796-123 Purdoux

NDC 81796-123 Purdoux

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81796-123?
  4. Purdoux Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
81796-123
Proprietary Name:
Purdoux
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Choice One Medical Inc
Labeler Code:
81796
Product Label ID:
c0a64276-c64a-3d5d-e053-2995a90afa26
Start Marketing Date: [9]
04-20-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 81796-123?

The NDC code 81796-123 is assigned by the FDA to the product Purdoux which is product labeled by Choice One Medical Inc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 81796-123-11 10 not applicable in 1 canister / 10 ml in 1 not applicable, 81796-123-12 35 not applicable in 1 canister / 35 ml in 1 not applicable, 81796-123-13 80 not applicable in 1 canister / 80 ml in 1 not applicable, 81796-123-14 130 not applicable in 1 canister / 130 ml in 1 not applicable, 81796-123-15 400 not applicable in 1 canister / 400 ml in 1 not applicable. 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 Purdoux?

Flip open dispensing cap. Locate wipe at center of roll via small opening of the lid. Close the lid cap after use. Apply to hands and skin. No rinsing required. Discard after use. Children under 6 years of age should be supervised when using this product.

Which are Purdoux UNII Codes?

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

Which are Purdoux 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".