NDC 74810-722 Clean Revolution

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:
74810-722
Proprietary Name:
Clean Revolution
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Replenish Bottling Llc
Labeler Code:
74810
Start Marketing Date: [9]
07-07-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74810-722-03

Package Description: 100 g in 1 BOTTLE, PLASTIC

NDC Code 74810-722-04

Package Description: 100 g in 1 BOTTLE, PUMP

Product Details

What is NDC 74810-722?

The NDC code 74810-722 is assigned by the FDA to the product Clean Revolution which is product labeled by Replenish Bottling Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74810-722-03 100 g in 1 bottle, plastic , 74810-722-04 100 g in 1 bottle, pump . 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 Clean Revolution?

1. Remove foil seal under cap.2. For best results , pour into Clean Revolution® Refillable Foaming Bottle. To create foam, product must be dispensed from a foaming pump. Product can also be dispensed in a liquid consistency using a standard pump or spray bottle. Never mix this product with other household ingredients or pour into a bottle that previously contained other chemicals.3. Apply sanitizer to palm. Rub the product over the surfaces of both hands until your hands are dry.

Which are Clean Revolution UNII Codes?

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

Which are Clean Revolution 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:

* Please review the disclaimer below.

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".