NDC 0116-2994 Scrub Care Exidine -4 Chg

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:
0116-2994
Proprietary Name:
Scrub Care Exidine -4 Chg
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Xttrium Laboratories, Inc.
Labeler Code:
0116
Start Marketing Date: [9]
11-01-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 0116-2994-01

Package Description: 3786 mL in 1 JUG

NDC Code 0116-2994-04

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC Code 0116-2994-05

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC Code 0116-2994-08

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC Code 0116-2994-16

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC Code 0116-2994-17

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC Code 0116-2994-32

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 0116-2994-33

Package Description: 946 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 0116-2994?

The NDC code 0116-2994 is assigned by the FDA to the product Scrub Care Exidine -4 Chg which is product labeled by Xttrium Laboratories, Inc.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 0116-2994-01 3786 ml in 1 jug , 0116-2994-04 118 ml in 1 bottle, plastic , 0116-2994-05 118 ml in 1 bottle, plastic , 0116-2994-08 237 ml in 1 bottle, plastic , 0116-2994-16 473 ml in 1 bottle, plastic , 0116-2994-17 473 ml in 1 bottle, plastic , 0116-2994-32 946 ml in 1 bottle, plastic , 0116-2994-33 946 ml in 1 bottle, plastic . 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 Scrub Care Exidine -4 Chg?

This product is used as Antiseptic . Surgical hand scrub: significantly reduces the number of microorganisms on the hand and forearms prior to surgery or patient care healthcare personnel hand wash: helps reduce bacteria that potentially can cause disease patient preoperative skin preparation: preparation of the patient’s skin prior to surgery skin wound and general skin cleansing

Which are Scrub Care Exidine -4 Chg UNII Codes?

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

Which are Scrub Care Exidine -4 Chg 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 Scrub Care Exidine -4 Chg?

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: 1661076 - Exidine 4 % Medicated Liquid Soap
  • RxCUI: 1661076 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap [Exidine]
  • RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Liquid Soap
  • RxCUI: 211365 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap
  • RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Surgical Scrub

* 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".