NDC 61037-421 Scrub, Scrub-stat

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:
61037-421
Proprietary Name:
Scrub, Scrub-stat
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bajaj Medical, Llc
Labeler Code:
61037
Start Marketing Date: [9]
07-22-1986
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 61037-421-01

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-02

Package Description: 118 mL in 1 BOTTLE

NDC Code 61037-421-03

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-04

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-05

Package Description: 473 mL in 1 BOTTLE, PUMP

NDC Code 61037-421-06

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-07

Package Description: 946 mL in 1 BOTTLE, PUMP

NDC Code 61037-421-08

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-09

Package Description: 237 mL in 1 BOTTLE, PUMP

NDC Code 61037-421-10

Package Description: 118 mL in 1 BOTTLE

NDC Code 61037-421-11

Package Description: 540 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-12

Package Description: 750 mL in 1 BOTTLE, PUMP

NDC Code 61037-421-13

Package Description: 750 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-14

Package Description: 59 mL in 1 BOTTLE

NDC Code 61037-421-15

Package Description: 800 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-16

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-17

Package Description: 946 mL in 1 BOTTLE, PUMP

NDC Code 61037-421-18

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-19

Package Description: 1000 mL in 1 POUCH

NDC Code 61037-421-20

Package Description: 1250 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-21

Package Description: 1250 mL in 1 BOTTLE, PUMP

NDC Code 61037-421-22

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-23

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC Code 61037-421-24

Package Description: 118 mL in 1 BOTTLE

NDC Code 61037-421-25

Package Description: 237 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 61037-421?

The NDC code 61037-421 is assigned by the FDA to the product Scrub, Scrub-stat which is product labeled by Bajaj Medical, Llc. The product's dosage form is . The product is distributed in 25 packages with assigned NDC codes 61037-421-01 118 ml in 1 bottle, plastic , 61037-421-02 118 ml in 1 bottle , 61037-421-03 237 ml in 1 bottle, plastic , 61037-421-04 473 ml in 1 bottle, plastic , 61037-421-05 473 ml in 1 bottle, pump , 61037-421-06 946 ml in 1 bottle, plastic , 61037-421-07 946 ml in 1 bottle, pump , 61037-421-08 3785 ml in 1 bottle, plastic , 61037-421-09 237 ml in 1 bottle, pump , 61037-421-10 118 ml in 1 bottle , 61037-421-11 540 ml in 1 bottle, plastic , 61037-421-12 750 ml in 1 bottle, pump , 61037-421-13 750 ml in 1 bottle, plastic , 61037-421-14 59 ml in 1 bottle , 61037-421-15 800 ml in 1 bottle, plastic , 61037-421-16 946 ml in 1 bottle, plastic , 61037-421-17 946 ml in 1 bottle, pump , 61037-421-18 1000 ml in 1 bottle, plastic , 61037-421-19 1000 ml in 1 pouch , 61037-421-20 1250 ml in 1 bottle, plastic , 61037-421-21 1250 ml in 1 bottle, pump , 61037-421-22 30 ml in 1 bottle, plastic , 61037-421-23 59 ml in 1 bottle, plastic , 61037-421-24 118 ml in 1 bottle , 61037-421-25 237 ml 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 Scrub, Scrub-stat?

Use with care in premature infants or infants under 2 months of age. These product may cause irritation or chemical burns.use full strengthdo not diluteSurgical hand scrub:remove jewelrywet hands and forearms with water and apply 5 mL of the productwash/scrub hands and forearms for 3 minutes paying particular attention to the nails, cuticles, and interdigital spacesrinse thoroughly with waterwash for an additional 3 minutes with 5 mL of the product and rinse under running waterdry thoroughlyHealthcare personnel handwashwet hands with waterdispense about 5 mL of product into cupped hands and wash in a vigorous manner for 30 secondsrinse and dry thoroughlySkin wound and general skin cleanserthoroughly rinse the area to be cleansed with waterapply the minimum amount of product necessary to cover the skin or wound area and wash gently. Rinse thoroughly with water.rinse again thoroughly

Which are Scrub, Scrub-stat UNII Codes?

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

Which are Scrub, Scrub-stat 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, Scrub-stat?

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: 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".