NDC 61037-421 Scrub, Scrub-stat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61037 - Bajaj Medical, Llc
- 61037-421 - Scrub, Scrub-stat
- 61037-421-01
- 61037-421-02
- 61037-421-03
- 61037-421-04
- 61037-421-05
- 61037-421-06
- 61037-421-07
- 61037-421-08
- 61037-421-09
- 61037-421-10
- 61037-421-11
- 61037-421-12
- 61037-421-13
- 61037-421-14
- 61037-421-15
- 61037-421-16
- 61037-421-17
- 61037-421-18
- 61037-421-19
- 61037-421-20
- 61037-421-21
- 61037-421-22
- 61037-421-23
- 61037-421-24
- 61037-421-25
- 61037-421 - Scrub, Scrub-stat
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?
What are the uses for Scrub, Scrub-stat?
Which are Scrub, Scrub-stat UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
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:
- COCAMINE OXIDE (UNII: QWA2IZI6FI)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- GLUCONIC ACID (UNII: R4R8J0Q44B)
- HYDROXYETHYL CELLULOSE (3000 CPS AT 1%) (UNII: 7Q6P4JN1QT)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- QUATERNIUM-33 (UNII: XPS4174QZJ)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Scrub, Scrub-stat?
- 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.
[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".