NDC 69804-089 Numbify Sanitize

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:
69804-089
Proprietary Name:
Numbify Sanitize
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ridge Properties
Labeler Code:
69804
Start Marketing Date: [9]
06-19-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69804-089-14

Package Description: 28500 mg in 1 BOTTLE, DISPENSING

NDC Code 69804-089-15

Package Description: 56700 mg in 1 BOTTLE, DISPENSING

NDC Code 69804-089-16

Package Description: 113400 mg in 1 BOTTLE, DISPENSING

Product Details

What is NDC 69804-089?

The NDC code 69804-089 is assigned by the FDA to the product Numbify Sanitize which is product labeled by Ridge Properties. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 69804-089-14 28500 mg in 1 bottle, dispensing , 69804-089-15 56700 mg in 1 bottle, dispensing , 69804-089-16 113400 mg in 1 bottle, dispensing . 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.

Which are Numbify Sanitize UNII Codes?

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

Which are Numbify 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:

What is the NDC to RxNorm Crosswalk for Numbify Sanitize?

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:
  • RxCUI: 2375042 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % Topical Gel
  • RxCUI: 2375042 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.04 MG/MG Topical Gel

* 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".