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NDC 76665-013 Pro-sanitize

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76665-013?
  4. Pro-sanitize 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:
76665-013
Proprietary Name:
Pro-sanitize
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clean Beauty Concepts
Labeler Code:
76665
Product Label ID:
b0e32307-5608-bd4c-e053-2a95a90a0985
Start Marketing Date: [9]
08-17-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 76665-013?

The NDC code 76665-013 is assigned by the FDA to the product Pro-sanitize which is product labeled by Clean Beauty Concepts. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76665-013-80 789 ml in 1 canister . 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 Pro-sanitize?

To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point and feed through dispenser holde in cover. Keep lid closed to prevent moisture loss.Open and unfold wipeThoroughly wipe hands, fingers and wrists. Be sure to use the entire wipe. Allow to dry.For dirty hands, use first wipe to clean hands, then discard wipe, sanitize with the second wipe.Discard after single useSupervise children under 6 years of age when using this product to avoid swallowing

Which are Pro-sanitize UNII Codes?

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

Which are Pro-sanitize 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".